draft by-law on registration, evaluation, authorization and restriction of chemicals first part general issues first section ai

DRAFT BY-LAW ON REGISTRATION, EVALUATION, AUTHORIZATION AND
RESTRICTION OF CHEMICALS
FIRST PART
General Issues
FIRST SECTION
Aim, Scope and Basis
Aim
ARTICLE 1 - (1) The purpose of this Bylaw is to ensure a high level of
protection of human health and the environment, including the
promotion of alternative methods for assessment of hazards of
substances while enhancing competitiveness and innovation.
Scope
ARTICLE 2 - (1) This Bylaw covers manufacturing, placing on the market
or use of the substances on their own, in a mixture or in an article
and placing the mixtures on the market.
(2) This Bylaw;
(a) shall not apply to the substances and mixtures below
1) Radioactive substances and mixtures within the scope of Bylaw on
the Safe Transportation of Radioactive Substances published in the
Official Gazette dated 08/07/2005 and numbered 25869;
2) Substances, on their own, in a mixture or in an article, which are
subject to customs supervision, provided that they do not undergo any
treatment or processing, and which are in temporary storage, or in a
free zone or free warehouse with a view to re- exportation, or in
transit;
3) Non-isolated intermediates;
4) The carriage of hazardous substances and hazardous mixtures by
rail, road, inland waterway, sea or air;
5) Wastes in the scope of the Bylaw on Waste Management published in
the Official Gazette dated 02/04/2015 and numbered 29314 and Bylaw on
Radioactive Waste Management published in the Official Gazette dated
09/03/2013 and numbered 28882.
6) Substances and mixtures which are manufactured or imported for the
purpose of defense
(3) of this Bylaw
a) The provisions of Second Part, Fifth Part, Sixth and Seventh Part
shall not apply to the substances manufactured or imported in order to
use in the products below:
1) Medicinal products for human or veterinary use within the scope of
Bylaw on the Licencing of Medicinal Products for Human Use published
in the Official Gazette dated 19/01/2005 and numbered 25705, Bylaw on
the Packaging and Labelling of Medicinal Products for Human Use
published in the Official Gazette dated 12/08/2005 andnumbered 25904
and Bylaw on Veterinary Medicinal Products published in the Official
Gazette dated 24/12/2012 and dated and numbered 28152;
2) Food within the scope of the Bylaw on Turkish Food Codex published
in the Official Gazette dated 29/12/2011 and numbered 28157;
3) Feeding stuffs within the scope of the Bylaw on Placing on the
Market and Use of Feeding Stuffs published in the Official Gazette
dated 27/12/2011 and numbered 28155;
(4) of this Bylaw:
(a) The provisions of Fourth Part shall not apply to the extent the
following mixtures in the finished state, intended for the final user:
1) Medicinal products for human or veterinary use within the scope of
Bylaw on the Licencing of Medicinal Products for Human Use published
in the Official Gazette dated 19/01/2005 and numbered 25705, Bylaw on
the Packaging and Labelling of Medicinal Products for Human Use and
published in the Official Gazette dated 12/08/2005 and numbered 25904
and Bylaw on Veterinary Medicinal Products published in the Official
Gazette dated 24/12/2012 and numbered 28152;
2) Cosmetic products within the scope of Bylaw on Cosmetics published
in the Official Gazette dated 23/05/2005 and numbered 25823;
3) Invasive medical devices or medical devices which can be used in
direct physical contact with the human body ;
4) Feeding stuffs within the scope of the Bylaw on Placing on the
Market and Use of Feeding Stuffs published in the Official Gazette
dated 27/12/2011 and numbered 28155.
5) Food within the scope of the Bylaw on Turkish Food Codex published
in the Official Gazette dated 29/12/2011 and numbered 28157;
(5) of this Bylaw:
(a) The following shall be exempted from Second Part, Fifth Part and
Sixth Part:
1) Substances included in Annex 4,
2) Substances included in Annex 5,
3) Substances on their own or in mixtures, registered in accordance
with Second Part , exported from Turkey by an actor in the supply
chain and re-imported into Turkey by the same or another actor in the
same supply chain who proofs that:
a) The substance being re-imported is the same as the exported
substance;
b) He has been provided with the information in accordance with
Articles 27 or 28 relating to the exported substance.
4) Substances, on their own, in mixtures or in articles, which have
been registered in accordance with Second Part and which are recovered
in Turkey if:
a) The substance that results from the recovery process is the same as
the substance that has been registered in accordance with Second Part;
and
b) The information required by Articles 27 or 28 relating to the
substance that has been registered in accordance with Second Part is
available to the establishment undertaking the recovery.
(6) of this Bylaw:
(a) Section 1 of Second Part , with the exception of Articles 9 and
10; and Seventh Part shall not be applied to the on-site isolated
intermediates and transported isolated intermediates.
(7) of this Bylaw:
(a) the provisions of the Second and Sixth Part shall not apply to the
polymers.
Legal Basis
ARTICLE 3 - (1) This By-law is prepared
a.
Based on the grounds of 09/08/1983 dated 2872 numbered
Environmental Law, 04/07/2011 dated 644 numbered Decree Law on
Establishment and Duties of Ministry of Environment and
Urbanization, 11/10/2011 dated 663 numbered Decree Law on
Establishment and Duties of Ministry of Health and Related
Authorities, 24/04/1930 dated 1593 numbered General Hygiene Law,
09/01/1985 dated 3146 numbered Law on Establishment and Duties of
Ministry of Labour and Social Security, 03/06/2011 dated 639
numbered Decree Law on Establishment and Duties of Ministry of
Food, Agriculture and Livestock, 11/06/2010 dated 5996 numbered
Law on Veterinary Services, Plant Health, Food and Feeding Stuff,
14/08/1987 dated 87/12028 numbered Regulation Promulgated by the
Cabinet of Ministers Decision on Production, Import,
Transportation, Storing, Warehousing, Sale, Use, Disposing,
Control of Explosives, Hunting Materials and Similar Materials
Outside the Scope of the Monopoly and 29/06/2001 dated and 4703
numbered Law on Preparation and Application of Technical
Regulations on Products.
SECOND SECTION
Definitions and General Provision
Definitions
ARTICLE 4 - (1) For the purposes of this Bylaw:
a) Alloy: means a metallic material, homogenous on a macroscopic
scale, consisting of two or more elements so combined that they cannot
be readily separated by mechanical means;
b) Downstream user: means any natural or legal person established
within Turkey, other than the manufacturer or the importer, who uses a
substance, either on its own or in a mixture, in the course of his
industrial or professional activities. A distributor or a consumer is
not a downstream user;
c) Intermediate: means a substance that is manufactured for and
consumed in or used for chemical processing in order to be transformed
into another substance
ç) Ministry: means the Ministry of Environment and Urbanization;
d) Identified use: means a use of a substance on its own or in a
mixture, or a use of a mixture, that is intended by an actor in the
supply chain, including his own use, or that is made known to him in
writing by a downstream user;
e) Scientific research and development: means any scientific
experimentation, analysis or chemical research carried out under
controlled conditions in a volume less than one tonne per year;
f) CAS Number: the number given by the “Chemical Abstract Service”;
g) Study summary: means a summary of the objectives, methods, results
and conclusions of a full study report providing sufficient
information to make an assessment of the relevance of the study;
ğ) Distributor: means any natural or legal person established within
Turkey, including a retailer, who only stores and places on the market
a substance, on its own or in a mixture , for third parties;
h)Substances which occur in nature: means a naturally occurring
substance as such, unprocessed or processed only by manual, mechanical
or gravitational means, by dissolution in water, by flotation, by
extraction with water, by steam distillation or by heating solely to
remove water, or which is extracted from air by any means;
ı) EINECS: European Inventory of Existing Commercial Chemical
Substances is the definer of all substances existing in the European
Community Market since 18th of September, 1981;
i) ELINCS: means all the new substances which are put on European
Community Market and have an ELINCS number by sending a notice to
European Inventory of Existing Commercial Chemical Substances after 18th
of September, 1981;
j) Article: means an object which during production is given a special
shape, surface or design which determines its function to a greater
degree than does its chemical composition;
k) Recipient of an article: means an industrial or professional user,
or a distributor, being supplied with an article but does not include
consumers;
l) Supplier of an article: means any producer or importer of an
article, distributor or other actor in the supply chain placing an
article on the market;
m) Manufacturer of an article: Natural or legal person established in
Turkey who manufacture or assembly the article;
n) IUPAC name: the name of the substance given by “International Union
and Pure Applied Chemistry”;
o) Relevant authority: means Ministry of Health for biocidal products,
Ministry of Customs and Trade for detergents and surface active agents
used in detergents, air aromatizing products, cleaning products with
strong acid or base and chemicals used in pool water, Ministry of
Food, Agriculture and Livestock for plant protection products,
Ministry of Science, Industry and Technology and Ministry of Internal
Affairs for explosives and pyrotechnic substances, Ministry of
Environment and Urbanization for all other substances and mixtures and
for the coordination of all the activities within the framework of
this Bylaw;
Ministry of Health, Ministry of Customs and Trade, Ministry of Food,
Agriculture and Livestock, Ministry of Science, Industry and
Technology, Ministry of Economy, Ministry of Work and Social Security,
Ministry of Energy and Natural Resources andMinistry of Environment
and Urbanization are responsible for inspection and enforcement of
restricted and prohibited substances in the scope of Annex 17..
ö) Manufacturing: means production or extraction of substances in the
natural state;
p) Manufacturer: means any natural or legal person established within
Turkey who manufactures a substance within Turkey;
r) Import: means the physical introduction into the customs territory
of Turkey;
s) Importer: means any natural or legal person established within
Turkey who is responsible for import;
ş) Non-isolated intermediate: means an intermediate that during
synthesis is not intentionally removed (except for sampling) from the
equipment in which the synthesis takes place.
t) Robust study summary: means a detailed summary of the objectives,
methods, results and conclusions of a full study report providing
sufficient information to make an independent assessment of the study
minimising the need to consult the full study report;
u) Mixture : means a mixture or solution composed of two or more
substances;
ü) Registrant: means the manufacturer or the importer of a substance
or the producer or importer of an article submitting a registration
for a substance;
v) Registrant's own use: means an industrial or professional use by
the registrant;
y) Restriction: means any condition for or prohibition of the
manufacture, use or placing on the market;
z) Not chemically modified substance: means a substance whose chemical
structure remains unchanged, even if it has undergone a chemical
process or treatment, or a physical mineralogical transformation, for
instance to remove impurities;
aa) SME: means small and medium-sized enterprises as defined in Bylaw
on Definition, Qualifications and Classification of Small and
Medium-sized Enterprises published in the Official Gazette dated
18/11/2005 numbered 25997;
bb) Use: means any processing, formulation, consumption, storage,
keeping, treatment, filling into containers, transfer from one
container to another, mixing, production of an article or any other
utilisation;
cc) Use and exposure category: means an exposure scenario covering a
wide range of processes or uses, where the processes or uses are
communicated, as a minimum, in terms of the brief general description
of use;
çç) Substance: means chemicals elements and their composition which
occur naturally or with a production including the additives in order
to keep the stability and impurities of production but excluding the
dissolvers removed without affecting the stability and the structure;
dd) Recipient of a substance or a mixture : means a downstream user or
a distributor being supplied with a substance or a mixture;
ee) Supplier of a substance or a mixture: means any manufacturer,
importer, downstream user or distributor placing on the market a
substance, on its own or in a mixture , or a mixture;
ff) Exposure scenario: means the set of conditions, including
operational conditions and risk management measures, that describe how
the substance is manufactured or used during its life-cycle and how
the manufacturer or importer controls, or recommends downstream users
to control, exposures of humans and the environment. These exposure
scenarios may cover one specific process or use or several processes
or uses as appropriate;
gg) Monomer: means a substance which is capable of forming covalent
bonds with a sequence of additional like or unlike molecules under the
conditions of the relevant polymer-forming reaction used for the
particular process;
ğğ) Placing on the market: means supplying or making available,
whether in return for payment or free of charge, to a third party or
import;
hh) Polymer: means a substance consisting of molecules characterised
by the sequence of one or more types of monomer units,distributed over
a range of molecular weights wherein differences in the molecular
weight are primarily attributable to differences in the number of
monomer units and comprises the following:
1.
A simple weight majority of molecules containing at least three
monomer units which are covalently bound to at least one other
monomer unit or other reactant; and
2.
Less than a simple weight majority of molecules of the same
molecular weight.
ıı) Full study report: means a complete and comprehensive description
of the activity performed to generate the information. This covers the
complete scientific paper as published in the literature describing
the study performed or the full report prepared by the test laboratory
describing the study performed;
ii) Transported isolated intermediate: means an intermediate not
meeting the criteria of a non-isolated intermediate and transported
between or supplied to other sites;
jj) Supplier: means any manufacturer, importer, downstream user or
distributor placing on the market a substance, on its own or in a
mixture , or a mixture;
kk) Actors in the supply chain: means all manufacturers and/or
importers and/or downstream users in a supply chain;
ll) Product and process orientated research and development: means any
scientific development related to product development or the further
development of a substance, on its own, in mixtures or in articles in
the course of which pilot plant or production trials are used to
develop the production process and/or to test the fields of
application of the substance;
mm) On-site: means a single location, in which, if there is more than
one manufacturer of (a) substance(s), certain infrastructure and
facilities are shared;
nn) On-site isolated intermediate: means an intermediate not meeting
the criteria of a non-isolated intermediate and where the manufacture
of the intermediate and the synthesis of (an)other substance(s) from
that intermediate take place on the same site, operated by one or more
legal entities;
oo) Competent authority: means Ministry of Environment and
Urbanization;
öö) Amount per year: means the avarege amount of manufacture or import
in the previous consecutive three calendar years, for the substances
that have been imported or manufactured for at least three consecutive
years; the amount of manufacture or import in the year of which the
highest quantity is imported or manufactured, for the substances that
have not been imported or manufactured for at least three consecutive
years;
General provisions
ARTICLE 5 – (1) Any manufacturer, importer and downstream users are
responsible with the production, placing on the market or use of the
substance without any negative effect to the human health or the
environment.
(2) Any manufacturer, importer, or where relevant downstream user,
may, whilst retaining full responsibility for complying with his
obligations under this Bylaw, appoint a third party representative for
all proceedings under Article 12, Article 19, Article 44 and Third
Part involving discussions with other manufacturers, importers, or
where relevant downstream users. In these cases, the identity of a
manufacturer or importer or downstream user who has appointed a
representative shall not be disclosed by the Ministry to other
manufacturers, importers, or, where relevant, downstream users.
SECOND PART
Registration of Substances
FIRST SECTION
Information Requirements and General Obligation to Register
Placing of the substances on the market
ARTICLE 6 – (1) Subject to Articles 7, 8 and 21, substances on their
own, in mixtures or in articles shall not be manufactured or placed on
the market unless they have been registered in accordance with the
relevant provisions of this Part where this is required.
General obligation to register substances on their own or in mixtures
ARTICLE 7 – (1) Save where this Regulation provides otherwise, any
manufacturer or importer of a substance, either on its own or in one
or more mixture (s), in quantities of one tons or more per year shall
submit a registration to the Ministry through Chemicals Registration
System in the website of Ministry.
2.
For monomers that are used as on-site isolated intermediates or
transported isolated intermediates, Articles 17 and 18 shall not
apply.
3.
Any manufacturer or importer of a polymer shall submit a
registration to the Ministry for the monomer substance(s) or any
other substance(s), that have not already been registered by an
actor up the supply chain, if both the following conditions are
met:
a.
The polymer consists of 2 % weight by weight (w/w) or more of such
monomer substance(s) or other substance(s) in the form of
monomeric units and chemically bound substance(s);
b.
The total quantity of such monomer substance(s) or other
substance(s) makes up one ton or more per year.
Registration and notification of substances in articles
ARTICLE 8 – (1) Any producer or importer of articles shall submit a
registration to the Ministry through Chemicals Registration System in
the website of Ministry for any substance contained in those articles,
if both the following conditions are met:
a.
The substance is present in those articles in quantities totaling
over one ton per producer or importer per year;
b.
The substance is intended to be released under normal or
reasonably foreseeable conditions of use.
2.
Any producer or importer of articles shall notify the Ministry
through Chemicals Registration System in the website of Ministry,
in accordance with paragraph 4 of this Article, if a substance
meets the criteria in Article 47 and defined in the article 49 if
both the following conditions are met:
a.
The substance is present in those articles in quantities
totaling over one ton per producer or importer per year;
b.
The substance is present in those articles above a concentration
of 0,1 % weight by weight (w/w);
2.
Paragraph 2 shall not apply where the producer or importer can
exclude exposure to humans or the environment during normal or
reasonably foreseeable conditions of use including disposal. In
such cases, the producer or importer shall supply appropriate
instructions to the recipient of the article.
3.
The information to be notified shall include the following:
a.
The identity and contact details of the producer or importer as
specified in section 1 of Annex 6, with the exception of their
own use sites;
b.
The registration number(s) referred to in Article 20(1), if
available;
c.
The identity of the substance as specified in sections 2.1 to
2.3.4 of Annex 6;
ç) Classification of the substance(s) as specified in sections 4.1 and
4.2 of Annex 6;
d) A brief description of the use(s) of the substance(s) in the
article as specified in section 3.5 of Annex 6 and of the uses of the
article(s);
e) The tonnage range of the substance(s) (1-10 tonnes; 10-100 tonnes;
100-1000 tonnes and more than 1000 tonnes)
2.
The Ministry may take decisions requiring producers or importers
of articles to submit a registration, for any substance in those
articles, if all the following conditions are met:
a.
The substance is present in those articles in quantities totalling
over one ton per producer or importer per year;
b.
The Ministry has grounds for suspecting that:
1) The substance is released from the articles, and
2) The release of the substance from the articles presents a risk to
human health or the environment;
c) the substance is not subject to paragraph 1
2.
Paragraphs 1 to 5 shall not apply to substances that have already
been registered for that use.
3.
Paragraphs 2, 3 and 4 of this Article shall apply six months after
a substance is identified in accordance with Article 49(1).
Only representative
ARTICLE 9 – (1)A natural or legal person established outside Turkey
who manufactures a substance on its own, in mixtures or in articles,
formulates a mixture or produces an article that is imported into the
Turkey may by mutual agreement appoint a natural or legal person
established in the Turkey to fulfil, as his only representative, the
obligations on importers under the scope of this Bylaw. Only
representative shall also comply with all obligations of importers
under this Regulation.
2.
The representative shall have a sufficient background in the
practical handling of substances and the information related to
them and, without prejudice to Article 32, shall keep available
and up-to-date information on quantities imported and customers
sold to, as well as information on the supply of the latest update
of the safety data sheet referred to in Article 27.
3.
If a representative is appointed in accordance with paragraphs 1
and 2, the non-resident manufacturer in Turkey shall inform the
importer(s) within the same supply chain of the appointment. These
importers shall be regarded as downstream users for the purposes
of this Bylaw.
Exemption from the general obligation to register for product and
process orientated research and development (PPORD)
ARTICLE 10 – (1) Articles 6, 7, 8, 17, 18 and 21 shall not apply for a
period of five years to a substance manufactured in the Turkey or
imported for the purposes of product and process orientated research
and development by a manufacturer or importer or producer of articles,
by himself or in cooperation with listed customers and in a quantity
which is limited to the purpose of product and process orientated
research and development.
2.
For the purpose of paragraph 1, the manufacturer or importer or
producer of articles shall notify the Ministry of the following
information:
a.
The identity of the manufacturer or importer or producer of
articles as specified in section 1 of Annex 6 ;
b.
The identity of the substance, as specified in section 2 of
Annex 6 ;
c.
The classification of the substance as specified in section 4 of
Annex 6 , if any;
ç) The estimated quantity as specified in section 3.1 of Annex 6 ;
d.
The list of customers referred to in paragraph 1, including
their names and addresses.
2.
The Ministry shall check the completeness of the information
supplied by the notifier and Article 20 (2) shall apply adapted as
necessary. The Ministry shall assign a number to the notification
and a notification date, which shall be the date of receipt of the
notification at the Ministry and shall forthwith communicate that
number and date to the manufacturer, or importer, or producer of
articles concerned.
3.
The Ministry may decide to impose conditions with the aim of
ensuring that the substance or the mixture or article in which the
substance is incorporated will be handled only by staff of listed
customers as referred to in paragraph 2(d) in reasonably
controlled conditions, in accordance with the requirements of
legislation for the protection of workers and the environment, and
will not be made available to the general public at any time
either on its own or in a mixture or article and may ask the
notifier to provide additional necessary information. Also, The
Ministry may re-collect remaining quantities following the
exemption period.
4.
In the absence of any indication to the contrary, the manufacturer
or importer of the substance or the producer or importer of
articles may manufacture or import the substance or produce or
import the articles not earlier than two weeks after the
notification.
5.
The Ministry may decide to extend the five-year exemption period
by a further maximum of five years or, in the case of substances
to be used exclusively in the development of medicinal products
for human or veterinary use, or for substances that are not placed
on the market, for a further maximum of ten years, upon request if
the manufacturer or importer or producer of articles can
demonstrate that such an extension is justified by the research
and development program.
Information to be submitted for general registration purposes
ARTICLE 11 – (1) A registration required by Article 7 or by Article
8(1) or (5) shall include all the following information:
a.
A technical dossier including:
1.
The identity of the manufacturer(s) or importer(s) as
specified in section 1 of Annex 6 ;
2.
The identity of the substance as specified in section 2 of
Annex 6 ;
3.
Information on the manufacture and use(s) of the substance as
specified in section 3 of Annex 6; this information shall
represent all the registrant's identified use(s). This
information may include, if the registrant deems appropriate,
the relevant use and exposure categories;
4.
The classification and labelling of the substance as specified
in section 4 of Annex 6 ;
5.
Guidance on safe use of the substance as specified in Section
5 of Annex 6 ;
6.
Study summaries of the information derived from the
application of Annexes 7 to 11;
7.
Robust study summaries of the information derived from the
application of Annexes 7 to 11,
8.
an indication as to which of the information submitted under
(3), (4), (6), (7) or subparagraph (b) has been reviewed by an
chemical assessment expert chosen by the manufacturer or
importer and certified according to Annex 18 of this Bylaw;
9.
Proposals for testing where listed in Annexes 9 and 10;
10.
For substances in quantities of 1 to 10 tons, exposure
information as specified in section 6 of Annex 6 ;
11.
A request as to which of the information in Article 61(2) the
manufacturer or importer considers should not be made
available on the Internet including a justification as to why
publication could be harmful for his or any other concerned
party's commercial interests.
b.
A chemical safety report when required under Article 15, in the
format specified in Annex 1. The relevant sections of this report
may include, if the registrant considers appropriate, the relevant
use and exposure categories.
c.
Save the cases in the scope of Article 23(3), Article 24(7) or
Article 26(3), the registrant shall have the legal ownership or
the right to refer to the summarised full study report intended
for registration according to paragraphs (1)(a)(6) and (1)(a)(7).
Joint submission of data by multiple registrants
ARTICLE 12 – (1)When a substance is intended to be manufactured by one
or more manufacturers and/or imported by one or more importers, and/or
is subject to registration under Article 8, the following shall apply:
a) Being subject to the paragraph 3 of this article, the information
specified in Article 11 (1) (a) (4), (6), (7) and (9), and any
relevant indication under Article 11 (1) (a) 8) is firstly presented
by the lead registrant. After this, each registrant will separately
present the information specified in Article 11 (1) (a) (1), (2), (3)
and (10) and the indication under Article 11 (1) (a) 8).
b) Each registrant may decide themselves whether to submit the
information specified in Article 11 (1) (a) 5) and any relevant
indication under Article 11 (1) (a) (8) separately himself or whether
by the lead registrant.
2.
Each registrant need only comply with paragraph 1 for items of
information specified in Article 11 (1) (a) (4), (6), (7) and (9)
that are required for the purposes of registration within his
tonnage band in accordance with Article 13.
3.
A registrant may submit the information referred to in Article 11
(1) (a) (4), (6), (7) or (9) separately if:
a.
It would be disproportionately costly for him to submit this
information jointly; or
b.
Submitting the information jointly would lead to disclosure of
information which he considers to be commercially sensitive and is
likely to cause him substantial commercial detriment; or
c.
He disagrees with the lead registrant on the selection of this
information.
(4) If the registrant complies with the provisions under paragraph 3,
he submits his justification with the register file.
Information to be submitted depending on tonnage
ARTICLE 13 – (1) The technical dossier referred to in Article 11 (1)
(a) shall include under points (6) and (7) of that provision all
physicochemical, toxicological and ecotoxicological information that
is relevant and available to the registrant and as a minimum the
following:
a.
The information specified in Annex 7 for substances meeting at
least one of the criteria specified in Annex 3, manufactured or
imported in quantities of one ton or more per year per
manufacturer or importer;
b.
The information on physicochemical properties specified in Annex
7, section 7 for substances manufactured or imported in
quantities of one ton or more per year per manufacturer or
importer which do not meet either of the criteria specified in
Annex 3;
c.
The information specified in Annexes 7 and 8 for substances
manufactured or imported in quantities of 10 tons or more per
year per manufacturer or importer;
ç) The information specified in Annexes 7 and 8 and testing proposals
for the provision of the information specified in Annex 9 for
substances manufactured or imported in quantities of 100 tons or more
per year per manufacturer or importer;
d.
Testing proposals for the provision of the information specified
in Annexes 7 and 8 and testing proposals for the provision of
the information specified in Annexes9 and 10 for substances
manufactured or imported in quantities of 1 000 tons or more per
year per manufacturer or importer.
2.
As soon as the quantity of a substance per manufacturer or
importer that has already been registered reaches the next tonnage
threshold, the manufacturer or importer shall inform the Ministry
in twenty working days of the additional information he would
require under paragraph 1.
3.
This Article shall apply to producers of articles adapted as
necessary.
General requirements for generation of information on intrinsic
properties of substances
ARTICLE 14 – (1) Information on intrinsic properties of substances may
be generated by means other than tests, provided that the conditions
set out in Annex 11 are met. In particular for human toxicity,
information shall be generated whenever possible by means other than
vertebrate animal tests, through the use of alternative methods, for
example, in vitro methods or qualitative or quantitative
structure-activity relationship models or from information from
structurally related substances (grouping or read-across). Testing in
accordance with Annex 8, Sections 8.6 and 8.7, Annex 9 and Annex 10
may be omitted where justified by information on exposure and
implemented risk management measures as specified in Annex 11.
(2) These methods shall be regularly reviewed and improved with a view
to reducing testing on vertebrate animals and the number of animals
involved.
(3) Where tests on substances are required to generate information on
intrinsic properties of substances, they shall be conducted in
accordance with the Bylaw on the Test Methods to Apply on Specifying
the Physico-Chemical, Toxicological, and Eco-Toxicological Properties
of the Substances and the Mixtures published in the Official Gazette
dated 11/12/2013 and numbered 28848 (bis). The information on the
intrinsic properties of chemical substances can be provided by the
other test methods provided that the conditions are met under Annex
11.
(4) Ecotoxicological and toxicological tests shall be carried out in
compliance with Bylaw on the Principles of Good Laboratory Practice,
Harmonization of Test Units, Inspection of Good Laboratory Practice
and Work published in the Official Gazette dated 9/3/2010 and numbered
27516.
(5) If a substance has already been registered, a new registrant shall
be entitled to refer to the study summaries or robust study summaries,
for the same substance submitted earlier, provided that he can show
that the substance that he is now registering is the same as the one
previously registered, including the degree of purity and the nature
of impurities, and that the previous registrant(s) have given
permission to refer to the full study reports for the purpose of
registration. A new registrant shall not refer to such studies in
order to provide the information required in Section 2 of Annex 6.
Chemical safety report and duty to apply and recommend risk reduction
measures
ARTICLE 15 – (1) Without prejudice to the Article 6 of Bylaw on Safety
and Security Measures related to Works with Chemical Substances
published in the Official Gazette dated 12/08/2013 and numbered 28733,
a chemical safety assessment shall be performed and a chemical safety
report completed for all substances subject to registration in
accordance with this Chapter in quantities of 10 tons or more per year
per registrant. The chemical safety report shall document the chemical
safety assessment which shall be conducted in accordance with
paragraphs 2 to 7 and with Annex I for either each substance on its
own or in a mixture or in an article or a group of substances.
2.
A chemical safety assessment in accordance with paragraph 1 need
not be performed for a substance which is present in a mixture if
the concentration of the substance in the mixture is less than the
lowest of any of the following:
a) The concentration threshold values that have been set Article 13 of
Bylaw on Classification, Labelling and Packaging of Substances and
Mixtures published in the Official Gazette dated 11/12/2013 and
numbered 28848.
b) 0,1 % weight by weight (w/w), if the substance meets the criteria
in Annex 13 of this Bylaw.
2.
A chemical safety assessment of a substance shall include the
following steps:
a.
Human health hazard assessment;
b.
Physicochemical hazard assessment;
c.
Environmental hazard assessment;
ç) Persistent, bioaccumulative and toxic (PBT) and very persistent and
very bioaccumulative (vPvB) assessment.
(4) If, as a result of carrying out steps (a) to (ç) of paragraph 3,
the registrant concludes that the substance fulfils the criteria of
PBT or vPvB or any of the following hazard classes or categories set
out in Annex 1 to the Bylaw on Classification, Labelling and Packaging
of Substances and Mixtures, the substance includes chemical safety
assessment exposure scenarios or exposure scenario assessment
including specifying the exposure scenario categories and exposure
scenario assumptions and the risk characterization. The exposure
scenarios (where appropriate the use and exposure categories),
exposure assessment and risk characterisation shall address all
identified uses of the registrant.
a.
Hazard classes 2.1 to 2.4, 2.6 and 2.7, 2.8 types A and B, 2.9,
2.10, 2.12, 2.13 categories 1 and 2, 2.14 categories 1 and 2,
2.15 types A to F;
b.
Hazard classes 3.1 to 3.6, 3.7 adverse effects on sexual
function and fertility or on development, 3.8 effects other than
narcotic effects, 3.9 and 3.10;
c.
Hazard class 4.1;
ç) Hazard class 5.1,
(5)The chemical safety report need not include consideration of the
risks to human health from the following end uses:
a.
In food contact materials within the scope Bylaw on the Turkish
Food Codex Substances and Materials in Contact with Food published
in the Official Gazette dated 29/12/2011 and numbered 28157;
b.
In cosmetic products within the scope of Bylaw on Cosmetics.
(6) Any registrant shall identify and apply the appropriate measures
to adequately control the risks identified in the chemical safety
assessment, and where suitable, recommend them in the Safety Data
Sheets which he supplies in accordance with Article 27.
(7)Any registrant required to conduct a chemical safety assessment
shall keep his chemical safety report available and up to date.
SECOND SECTION
Substances Regarded as Being Registered
Substances in plant protection and biocidal products
ARTICLE 16 – (1) Active substances and co-formulants manufactured or
imported for use in plant protection products only and included the
Bylaw on Licensing of Plant Protection Products published in the
Official Gazette dated 25/03/2011 numbered 27885 and Bylaw on the
Classification, Packaging and Labelling of Plant Protection Products
published in the Official Gazette dated 23/03/2010 and numbered 27530
shall be regarded as being registered and the registration as
completed for manufacture or import for the use as a plant protection
product and therefore as fulfilling the requirements of Section 1 of
Part 2.
2.
Active substances manufactured or imported for use in biocidal
products only and included in Bylaw on Biocidal Products published
in the Official Gazette dated 31/12/2009 numbered 27449 (4th bis)
on the placing of biocidal products on the market, shall be
regarded as being registered and the registration as completed for
manufacture or import for the use in a biocidal product and
therefore as fulfilling the requirements of Section 1 of this
Part.
THIRD SECTION
Obligation to Register and Information Requirements for Certain Types
of Isolated Intermediates
Registration of on-site isolated intermediates
ARTICLE 17 – (1) Any manufacturer of an on-site isolated intermediate
in quantities of one ton or more per year shall submit a registration
to the Ministry through Chemicals Registration System in the website
of Ministry for the on-site isolated intermediate.
2.
A registration for an on-site isolated intermediate shall include
all the following information, to the extent that the manufacturer
is able to submit it without any additional testing:
a.
The identity of the manufacturer as specified in Section 1 of
Annex 6 ;
b.
The identity of the intermediate as specified in Sections 2.1 to
2.3.4 of Annex 6 ;
c.
The classification of the intermediate as specified in Section 4
of Annex 6 ;
ç) Any available existing information on physicochemical, human health
or environmental properties of the intermediate. Where a full study
report is available, a study summary shall be submitted;
d.
A brief general description of the use, as specified in Section
3.5 of Annex 6 ;
e.
Details of the risk management measures applied.
2.
Paragraph 2 shall apply only to on-site isolated intermediates if
the manufacturer confirms that the substance is only manufactured
and used under strictly controlled conditions in that it is
rigorously contained by technical means during its whole
lifecycle. Control and procedural technologies shall be used to
minimise emission and any resulting exposure. If these conditions
are not fulfilled, the registration shall include the information
specified in Article 11.
3.
Save the cases in the scope of Article 23(3), 24 (7) or 26 (3),
according to the paragraph (2)(ç) registrant shall have permission
to the ownership or the right to refer to the full study report
for purpose of registration.
Registration of transported isolated intermediates
ARTICLE 18 – (1) Any manufacturer or importer of a transported
isolated intermediate in quantities of one ton or more per year shall
submit a registration to the Ministry through Chemicals Registration
System in the website of Ministry for the transported isolated
intermediate.
2.
A registration for a transported isolated intermediate shall
include all the following information:
a.
The identity of the manufacturer or importer as specified in
Section 1 of Annex 6 ;
b.
The identity of the intermediate as specified in Sections 2.1 to
2.3.4 of Annex 6 ;
c.
The classification of the intermediate as specified in Section 4
of Annex 6 ;
ç) Any available existing information on physicochemical, human health
or environmental properties of the intermediate. Where a full study
report is available, a study summary shall be submitted;
d) A brief general description of the use, as specified in Section 3.5
of Annex 6;
e) Information on risk management measures applied and recommended to
the user in accordance with paragraph 4.
2.
A registration for a transported isolated intermediate in
quantities of more than 1 000 tons per year per manufacturer or
importer shall include the information specified in Annex 7 in
addition to the information required under paragraph 2. For the
generation of this information, Article 14 shall apply.
3.
Paragraphs 2 and 3 shall apply only to transported isolated
intermediates if the manufacturer or importer confirms himself or
states that he has received confirmation from the user that the
synthesis of (an)other substance(s) from that intermediate takes
place on other sites under the following strictly controlled
conditions:
a.
The substance is rigorously contained by technical means during
its whole lifecycle including manufacture, purification,
cleaning and maintenance of equipment, sampling, analysis,
loading and unloading of equipment or vessels, waste disposal or
purification and storage. If these conditions are not fulfilled,
the registration shall include the information specified under
Article 11
b.
Procedural and control technologies shall be used that minimize
emission and any resulting exposure;
c.
Only properly trained and authorized personnel handle the
substance;
ç) In the case of cleaning and maintenance works, special procedures
such as purging and washing are applied before the system is opened
and entered;
d) In cases of accident and where waste is generated, procedural
and/or control technologies are used to minimize emissions and the
resulting exposure during purification or cleaning and maintenance
procedures;
e) Substance-handling procedures are well documented and strictly
supervised by the site operator.
(5) Save the cases in the scope of Article 23(3), 24 (7) or 26 (3),
according to the paragraph (2)(ç) registrant shall have permission to
the ownership or the right to refer to the full study report for
purpose of registration.
Joint submission of data on isolated intermediates by multiple
registrants
ARTICLE 19 – (1) When an on-site isolated intermediate or transported
isolated intermediate is intended to be manufactured by one or more
manufacturers and/or imported by one or more importers, the following
shall apply.
Subject to paragraph 2 of this Article, the information specified in
Article 17(2)(c) and (ç) and Article 18(2) (c) and (ç) shall first be
submitted by one manufacturer or importer acting with the agreement of
the other assenting manufacturer(s) or importer(s) (hereinafter
referred to as ‘the lead registrant’). Each registrant shall
subsequently submit separately the information specified in Article
17(2) (a), (b), (d) and (e) and Article 18(2) (a), (b), (d) and (e).
2.
A manufacturer or importer may submit the information referred to
in Article 17(2)(c) or (ç) and Article 18 (2) (c) or (ç)
separately if:
a.
It would be disproportionately costly for him to submit this
jointly; or
b.
Submitting the information jointly would lead to disclosure of
information which he considers to be commercially sensitive and
is likely to cause him substantial commercial detriment; or
c.
He disagrees with the lead registrant on the selection of this
information.
3) If paragraph 2apply, the manufacturer or importer shall submit,
along with the dossier, an explanation as to why the costs would be
disproportionate, why disclosure of information was likely to lead to
substantial commercial detriment, or the nature of the disagreement,
as the case may be.
FOURTH SECTION
Common Provisions for All Registrants
Duties of Ministry
ARTICLE 20 – (1) The Ministry shall assign a submission number to each
registration, which is to be used for all correspondence regarding the
registration until the registration is deemed to be complete, and a
submission date, which shall be the date of receipt of the
registration at the Ministry.
2.
In respect to registration dossier
(a) The Ministry shall undertake a completeness check of each
registration in order to ascertain that all the elements required
under Articles 11 and 13 or under Articles 17 or 18 as well as the
registration fee referred to in Article 59 have been provided. The
completeness check shall not include an assessment of the quality or
the adequacy of any data or justifications submitted.
(b)The Ministry shall undertake the completeness check within three
weeks of the submission date. If a registration is incomplete, the
Ministry shall inform the registrant, before expiry of the three-week
period, as to what further information is required in order for the
registration to be complete, while setting a deadline for this.
(c)The registrant shall complete his registration and submit it to the
Ministry within the deadline set. The Ministry shall confirm the
submission date of the further information to the registrant. The
Ministry shall perform a further completeness check, considering the
further information submitted.
(ç)The Ministry shall reject the registration if the registrant fails
to complete his registration within the deadline set. The registration
fee shall not be reimbursed in such cases.
2.
Once the registration is complete, the Ministry shall assign a
registration number to the substance concerned and a registration
date, which shall be the same as the submission date. The Ministry
shall communicate the registration number and registration date to
the registrant concerned. The registration number shall be used
for all subsequent correspondence regarding registration.
3.
Where additional information for a particular substance is
submitted to the Ministry by a new registrant, the Ministry shall
notify the existing registrants that this information is available
on the database for the purposes of Article 22.
Manufacturing and import of substances
ARTICLE 21- (1)A registrant may start or continue the manufacture or
import of a substance or production or import of an article, if there
is no indication to the contrary from the Ministry in accordance with
Article 20(2) within the three weeks after the submission date,
without prejudice to Article 24(8).
In the case of an update of a registration according to Article 22, a
registrant may continue the manufacture or import of the substance, or
the production or import of the article, if there is no indication to
the contrary from the Ministry in accordance with Article 20(2) within
the three weeks after the update date, without prejudice to Article
24(8).
2.
If the Ministry has informed the registrant that he is to submit
further information the registrant may start the manufacture or
import of a substance or production or import of an article if
there is no indication to the contrary from the Ministry within
the three weeks after receipt by the Ministry of the further
information necessary to complete his registration, without
prejudice to Article 24 (8).
3.
If a lead registrant submits parts of the registration on behalf
of one or more other registrants, as provided for in Articles 12
or 19, any of the other registrants may manufacture or import the
substance or produce or import the articles only after the expiry
of the time-limit laid down in paragraph 1 or 2 of this Article
and provided that there is no indication to the contrary from the
Ministry in respect of the registration of the lead registrant
acting on behalf of the others and his own registration.
Further duties of registrants
ARTICLE 22 – (1) Following registration, a registrant shall be
responsible on his own initiative for updating his registration
without undue delay with relevant new information and submitting it to
the Ministry in the following cases:
a.
Any change in his status, such as being a manufacturer, an
importer or a producer of articles, or in his identity, such as
his name or address;
b.
Any change in the composition of the substance as given in Section
2 of Annex 6 ;
c.
Changes in the annual or total quantities manufactured or imported
by him or in the quantities of substances present in articles
produced or imported by him if these result in a change of tonnage
band, including cessation of manufacture or import;
ç) New identified uses and new uses advised against as in Section 3.7
of Annex 6 for which the substance is manufactured or imported;
d) New knowledge of the risks of the substance to human health and/or
the environment of which he may reasonably be expected to have become
aware which leads to changes in the safety data sheet or the chemical
safety report;
e) Any change in the classification and labelling of the substance;
f) Any update or amendment of the chemical safety report or Section 5
of Annex 6 ;
g) The registrant identifies the need to perform a test listed in
Annex 9 or Annex 10, in which cases a testing proposal shall be
developed;
ğ) Any change in the access granted to information in the
registration.
2.
A registrant shall submit to the Ministry an update of the
registration containing the information required by the decision
made in accordance with Articles 36, 37, 41 or 50 within the
deadline specified in that decision.
3.
The Ministry shall undertake a completeness check of each updated
registration according to Article 20(2) (a) and 20 (2) (b). In
cases where the update is in accordance with Article 13(2) and
with paragraph 1(c) of this Article then the Ministry shall check
the completeness of the information supplied by the registrant and
Article 20(2) shall apply adapted as necessary.
4.
In cases covered by Articles 12 or 19, each registrant shall
submit separately the information specified in paragraph 1(c) of
this Article.
THIRD PART
Data Sharing and Avoidance of Unnecessary Testing
FIRST SECTION
Data Sharing Rules
ARTICLE 23 – (1) In order to avoid animal testing, testing on
vertebrate animals for the purposes of this Bylaw shall be undertaken
only as a last resort. It is also necessary to take measures limiting
duplication of other tests.
(2) The sharing and joint submission of information in accordance with
this Bylaw shall concern technical data and in particular information
related to the intrinsic properties of substances. Registrants shall
refrain from exchanging information concerning their market behaviour,
in particular as regards production capacities, production or sales
volumes, import volumes or market shares.
(3) Any study summaries or robust study summaries of studies submitted
in the framework of a registration at least 12 years previously can be
used for the purposes of registration by another manufacturer or
importer.
SECOND SECTION
Sharing the Existing Data
Sharing the existing data for registered substances
ARTICLE 24 – (1) Every potential registrant of a substance shall
inquire from the Ministry through Chemicals Registration System in the
website of Ministry from 31/12/2023 whether a registration has already
been submitted for the same substance. He shall submit all the
following information to the Ministry with the inquiry:
a.
his identity as specified in Section 1 of Annex 6, with the
exception of the use sites;
b.
the identity of the substance, as specified in Sections 2.1 to
2.3.4 of Annex 6;
c.
which information requirements would require studies involving
vertebrate animals to be carried out by him;
(2)Where a substance has previously been registered less than 12 years
earlier, potential registrant shall require nessessary information
with respect to the Article 11 (a) (6) and (7) from the previous
registrant(s) in order to register
a.
Shall, in the case of information involving tests on vertebrate
animals; and
a.
May, in the case of information not involving tests on vertebrate
animals.
(3) When a request for information has been made according to
paragraph 1, the potential and the previous registrant(s) as referred
to in paragraph 1 shall make every effort to reach an agreement on the
sharing of the information requested by the potential registrant(s)
with respect to Article 11 (a) (6) and (7).
(4) The previous registrant and potential registrant(s) shall make
every effort to ensure that the costs of sharing the information are
determined in a fair, transparent and non-discriminatory way.
Registrants are only required to share in the costs of information
that they are required to submit to satisfy their registration
requirements.
(5) On agreement on the sharing of the information, the previous
registrant shall make available to the new registrant the agreed
information and shall give the new registrant the permission to refer
to the previous registrant's full study report.
(6) If there is failure to reach such an agreement, the potential
registrant(s) shall inform the Ministry and the previous registrant(s)
thereof at the earliest one month after receipt, from the Ministry, of
the name and address of the previous registrant(s).
(7) Within one month from the receipt of the information referred to
in paragraph 5, the Ministry shall give the potential registrant
permission to refer to the information requested by him in his
registration dossier, subject to the potential registrant providing,
upon request by the Ministry, proof that he has paid the previous
registrant(s) for that information a share of cost incurred. The
previous registrant(s) shall have a claim on the potential registrant
for a proportionate share of the cost incurred by him. Calculation of
the proportionate share may be facilitated by the guidance adopted by
the Ministry. Provided he makes the full study report available to the
potential registrant, the previous registrant(s) shall have a claim on
the potential registrant for an equal share of the cost incurred by
him, which may be enforceable in the national courts.
(8) The registration waiting period in accordance with Article 21(1)
for the new registrant shall be extended by a period of four months,
if the previous registrant so requests.
THIRD SECTION
Rules for the Substances
Substance Information Exchange Forums
ARTICLE 25 – (1) All potential registrants, downstream users and third
parties of substance who have submitted pre-substance information
exchange forum (pre SIEF) to the Ministry, or registrants who have
submitted a registration for that substance before 31/12/2023 shall be
participants in a substance information exchange forum (SIEF).
(2) The aim of each SIEF shall be to:
a.
Facilitate, for the purposes of registration, the exchange of
the information specified in Article 11 (1) (a) (6) and (7)
between potential registrants, thereby avoiding the duplication
of studies; and
b.
Agree classification and labelling where there is a difference
in the classification and labelling of the substance between
potential registrants.
(3)SIEF participants shall provide other participants with existing
studies, react to requests by other participants for information,
collectively identify needs for further studies for the purposes of
paragraph 2(a) and arrange for such studies to be carried out. Each
SIEF shall be operational until 31/12/2025.
Sharing of data involving tests
ARTICLE 26 – (1) Before testing is carried out in order to meet the
information requirements for the purposes of registration, a SIEF
participant shall inquire whether a relevant study is available by
communicating within his SIEF. If a relevant study involving tests on
vertebrate animals is available within the SIEF, a participant of that
SIEF shall request that study. If a relevant study not involving tests
on vertebrate animals is available within the SIEF, a SIEF participant
may request that study. Within one month of the request, the owner of
the study shall provide proof of its cost to the participant(s)
requesting it. The participant(s) and the owner shall make every
effort to ensure that the costs of sharing the information are
determined in a fair, transparent and non-discriminatory way. The
calculation of the proportional cost sharing may be facilitated by the
Ministry’s advice. If they cannot reach such an agreement, the cost
shall be shared equally. The owner shall give permission to refer to
the full study report for the purpose of registration within two weeks
of receipt of payment. Registrants are only required to share in the
costs of information that they are required to submit to satisfy their
registration requirements.
2.
If a relevant study involving tests is not available within the
SIEF, only one study shall be conducted per information
requirement within each SIEF by one of its participants acting on
behalf of the others. They shall take all reasonable steps to
reach an agreement within a deadline set by the Ministry as to who
is to carry out the test on behalf of the other participants and
to submit a summary or robust study summary to the Ministry. If no
agreement is reached, the Ministry shall specify which registrant
or downstream user shall perform the test. All participants of the
SIEF who require a study shall contribute to the costs for the
elaboration of the study with a share corresponding to the number
of participating potential registrants. Those participants that do
not carry out the study themselves shall have the right to receive
the full study report within two weeks following payment to the
participant that carried out the study.
3.
If the owner of a study as referred to in paragraph 1 which
involves testing on vertebrate animals refuses to provide either
proof of the cost of that study or the study itself to (an) other
participant(s), he shall not be able to proceed with registration
until he provides the information to the other participants(s).
The other participant(s) shall proceed with registration without
fulfilling the relevant information requirement, explaining the
reason for this in the registration dossier. The study shall not
be repeated unless within 12 months of the date of registration of
the other participant(s), the owner of this information has not
provided it to them and the Ministry decides that the test should
be repeated by them. However, if a registration containing this
information has already been submitted by another registrant, the
Ministry shall give the other participant(s) permission to refer
to the information in his registration dossier(s). The other
registrant shall have a claim on the other participant(s) for an
equal share of the cost, provided he makes the full study report
available to the other participant(s), which may be enforceable in
the national courts.
4.
If the owner of a study as referred to in paragraph 1 which does
not involve testing on vertebrate animals refuses to provide
either proof of the cost of that study or the study itself to
(an)other participant(s), the other SIEF participants shall
proceed with registration as if no relevant study was available in
the SIEF.
5.
The owner of the study who has refused to provide either proof of
the cost or the study itself, as referred to in paragraph 3 or 4
of this Article, shall be penalized in accordance with Article 63.
FOURTH PART
Information in the Supply Chain
Requirements for safety data sheets
ARTICLE 27 – (1) The supplier of a substance or a mixture shall
provide the recipient of the substance or mixture with a safety data
sheet compiled in accordance with Annex 2 and prepared by a certified
chemicals assessment expert according to Annex 18:
a.
Where a substance or a mixture meets the criteria for
classification as hazardous in accordance with the Bylaw on
Classification, Labelling and Packaging of Substances and
Mixtures or
b.
Where a substance is persistent, bio accumulative and toxic or
very persistent and very bio accumulative in accordance with the
criteria set out in Annex 13; or
c.
Where a substance is included in the list established in
accordance with Article 49 for reasons other than those referred
to in points (a) and (b).
2.
Any actor in the supply chain who is required, under Articles 15
or 33 to carry out a chemical safety assessment for a substance
shall ensure that the information in the safety data sheet is
consistent with the information in this assessment. If the safety
data sheet is developed for a mixture and the actor in the supply
chain has prepared a chemical safety assessment for that mixture,
it is sufficient if the information in the safety data sheet is
consistent with the chemical safety report for the mixture instead
of with the chemical safety report for each substance in the
mixture.
3.
The supplier shall provide the recipient at his request with a
safety data sheet compiled in accordance with Annex 2, where a
mixture does not meet the criteria for classification as hazardous
in accordance with Bylaw on Classification, Labelling and
Packaging of Substances and Mixtures, but contains:
a.
In an individual concentration of ≥ 1 % by weight for
non-gaseous mixtures and ≥ 0,2 % by volume for gaseous mixtures
at least one substance posing human health or environmental
hazards; or
b.
In an individual concentration of ≥ 0,1 % by weight for
non-gaseous mixtures at least one substance that is carcinogenic
category 2 or toxic to reproduction category 1, respiratory
sensitiser category 1 or is persistent, bio accumulative and
toxic or very persistent and very bio accumulative in accordance
with the criteria set out in Annex 13 or has been included for
reasons other than those referred to in point (a) in the list
established in accordance with Article 49(1);
c.
A substance for which there is workplace exposure limits.
2.
The safety data sheet need not be supplied where substances that
are hazardous offered or sold to the general public, are provided
with sufficient information to enable users to take the necessary
measures as regards the protection of human health, safety and the
environment, unless requested by a downstream user or distributor.
3.
The safety data sheet shall be supplied in Turkish.
4.
The safety data sheet shall be dated and shall contain the
following headings:
a.
Identification of the substance/ mixture and of the
company/undertaking;
b.
Hazards identification;
c.
Composition/information on ingredients;
ç) First-aid measures;
d.
Fire-fighting measures;
e.
Accidental release measures;
f.
Handling and storage;
g.
Exposure controls/personal protection;
ğ) Physical and chemical properties;
h.
Stability and reactivity;
ı) Toxicological information;
i.
Ecological information;
j.
Disposal considerations;
k.
Transport information;
l.
Regulatory information;
m.
Other information.
2.
Any actor in the supply chain who is required to prepare a
chemical safety report according to Articles 15 or 33 shall place
the relevant exposure scenarios (including use and exposure
categories where appropriate) in an annex to the safety data sheet
covering identified uses and including specific conditions
resulting from the application of Section 3 of Annex 11.
Any downstream user shall include relevant exposure scenarios, and use
other relevant information, from the safety data sheet supplied to him
when compiling his own safety data sheet for identified uses.
Any distributor shall pass on relevant exposure scenarios, and use
other relevant information, from the safety data sheet supplied to him
when compiling his own safety data sheet for uses for which he has
passed on information according to Article 33(2).
(8) A safety data sheet shall be provided free of charge on paper or
electronically.
(9) Suppliers shall update the safety data sheet without delay on the
following occasions:
a.
As soon as new information which may affect the risk management
measures, or new information on hazards becomes available;
b.
Once an authorization has been granted or refused;
c.
Once a restriction has been imposed.
(10) The new, dated version of the information, shall be provided free
of charge on paper or electronically to all former recipients to whom
they have supplied the substance or mixture within the preceding 12
months. Any updates following registration shall include the
registration number.
(11) The safety data sheets for substances shall contain the
classification according to Bylaw on Classification, Labelling and
Packaging of Substances and Mixtures.
Duty to communicate information down the supply chain for substances
on their own or in mixtures for which a safety data sheet is not
required
ARTICLE 28 – (1) Any supplier of a substance on its own or in a
mixture who does not have to supply a safety data sheet in accordance
with Article 27 shall provide the recipient with the following
information:
a.
The registration number(s) referred to in Article 20(3), if
available, for any substances for which information is
communicated under this paragraph;
b.
If the substance is subject to authorization and details of any
authorization granted or denied under Part 7 in this supply
chain;
c.
Details of any restriction imposed under Part 8;
ç) Any other available and relevant information about the substance
that is necessary to enable appropriate risk management measures to be
identified and applied including specific conditions resulting from
the application of Section 3 of Annex 11.
2.
The information referred to in paragraph 1 shall be communicated
free of charge on paper or electronically at the latest at the
time of the first delivery of a substance on its own or in a
mixture after the enforcement date.
3.
Suppliers shall update this information without delay on the
following occasions:
a.
As soon as a new information which may affect the risk
management measures, or new information on hazards becomes
available;
b.
Once an authorization has been granted or refused;
c.
Once a restriction has been imposed.
(4)In addition, the updated information shall be provided free of
charge on paper or electronically to all former recipients to whom
they have supplied the substance or mixture within the preceding 12
months. Any updates following registration shall include the
registration number.
Duty to communicate information on substances in articles
ARTICLE 29 – (1) Any supplier of an article containing a substance
meeting the criteria in Article 47 in a concentration above 0,1 %
weight by weight (w/w) shall provide the recipient of the article with
sufficient information, available to the supplier, to allow safe use
of the article including, as a minimum, the name of that substance
with respect to the Article 49 (1).
(2) On request by a consumer any supplier of an article containing a
substance meeting the criteria in Article 47 in a concentration above
0,1 % weight by weight (w/w) shall provide the consumer with
sufficient information, available to the supplier, to allow safe use
of the article including, as a minimum, the name of that substance
with respect to the Article 49 (1).The relevant information shall be
provided, free of charge, within 45 days of receipt of the request.
Duty to communicate information on substances and mixtures up the
supply chain
ARTICLE 30 – (1) Any actor in the supply chain of a substance or a
mixture shall communicate the following information to the next actor
or distributor up the supply chain:
a.
New information on hazardous properties, regardless of the uses
concerned;
b.
Any other information that might call into question the
appropriateness of the risk management measures identified in a
safety data sheet supplied to him, which shall be communicated
only for identified uses.
Access to information for workers
ARTICLE 31 – (1) Workers and their representatives shall be granted
access by their employer to the information provided in accordance
with Articles 27 and 28 in relation to substances or mixtures that
they use or may be exposed to in the course of their work.
Obligation to keep information
ARTICLE 32 – (1) Each manufacturer, importer, downstream user and
distributor shall assemble and keep available all the information he
requires to carry out his duties under this Bylaw for a period of at
least 10 years after he last manufactured, imported, supplied or used
the substance or mixture. That manufacturer, importer, downstream user
or distributor shall submit this information or make it available
without delay upon request to the Ministry without prejudice to Parts
2 and 6.
2.
In the event of a registrant, downstream user or distributor
ceasing activity, or transferring part or all of his operations to
a third party, the party responsible for liquidating the
registrant, downstream user or distributor's undertaking or
assuming responsibility for the placing on the market of the
substance or mixture concerned shall be bound by the obligation in
paragraph 1 in place of the registrant, downstream user or
distributor.
FIFTH PART
Downstream Users
Downstream user chemical safety assessments and duty to identify,
apply and recommend risk reduction measures
ARTICLE 33 – (1) A downstream user or distributor may provide
information to assist in the preparation of a registration.
2.
In respect to communication of information
(a) Any downstream user shall have the right to make a use, as a
minimum the brief general description of use, known in writing (on
paper or electronically) to the manufacturer, importer, downstream
user or distributor who supplies him with a substance on its own or in
a mixture with the aim of making this an identified use.
(b) In making a use known, he shall provide sufficient information to
allow the manufacturer, importer or downstream user who has supplied
the substance, to prepare an exposure scenario, or if appropriate a
use and exposure category, for his use in the manufacturer, importer
or downstream user's chemical safety assessment.
(c) Distributors shall pass on such information to the next actor or
distributor up the supply chain. Downstream users in receipt of such
information may prepare an exposure scenario for the identified
use(s), or pass the information to the next actor up the supply chain.
(3) For registered substances, the manufacturer, importer or
downstream user may request the manufacturer, importer or downstream
user,to add the substance on identified use in accordance with
paragraph 2. Provided that the request was made at least one month
before the supply, either before he next supplies or within one month
after the request, whichever is the later, shall apply the duties of
Article 15.
(4) A downstream user of a substance on its own or in a mixture shall
prepare a chemical safety report in accordance with Annex 12 for any
use outside the conditions described in an exposure scenario or if
appropriate a use and exposure category communicated to him in a
safety data sheet or for any use his supplier advises against.
A downstream user need not prepare such a chemical safety report in
any of the following cases:
a.
A safety data sheet is not required to be communicated with the
substance or mixture in accordance with Article 27;
b.
A chemical safety report is not required to be completed by his
supplier in accordance with Article 15;
c.
The downstream user uses the substance or mixture in a total
quantity of less than one ton per year;
ç) The downstream user implements or recommends an exposure scenario
which includes as a minimum the conditions described in the exposure
scenario communicated to him in the safety data sheet;
d.
The substance is present in a mixture in a concentration lower
than any of the concentrations set out in Article 15(2);
e.
The downstream user is using the substance for the purposes of
product and process oriented research and development, provided
that the risks to human health and the environment are
adequately controlled in accordance with the requirements of
legislation for the protection of workers and the environment.
(5) Any downstream user shall identify, apply and where suitable,
recommend, appropriate measures to adequately control risks identified
in any of the following:
a.
The safety data sheet(s) supplied to him;
b.
His own chemical safety assessment;
c.
Any information on risk management measures supplied to him in
accordance with Article 28.
(6) Where a downstream user does not prepare a chemical safety report
in accordance with paragraph 4(c), he shall consider the use(s) of the
substance and identify and apply any appropriate risk management
measures needed to ensure that the risks to human health and the
environment are adequately controlled. Where necessary, this
information shall be included in any safety data sheet prepared by
him.
(7) Downstream users shall keep their chemical safety report up to
date and available.
(8)A chemical safety report prepared in accordance with paragraph 4 of
this Article need not include consideration of the risks to human
health from the end uses set out in Article 15(5).
Obligation for downstream users to report information
ARTICLE 34 – (1) Before commencing or continuing with a particular use
of a substance that has been registered by an actor up the supply
chain in accordance with Articles 7 or 18, the downstream user shall
report to the Ministry the information specified in paragraph 2 of
this Article, in the following cases:
a.
The downstream user has to prepare a chemical safety report in
accordance with Article 33(4); or
b.
The downstream user is relying on the exemptions in Article
33(4)(c) or (e).
2.
The information reported by the downstream user shall include the
following:
a.
His identity and contact details as specified in Section 1.1 of
Annex 6 ;
b.
The registration number(s) referred to in Article 20(3), if
available;
c.
The identity of the substance(s) as specified in Section 2.1 to
2.3.4 of Annex 6 ;
ç) The identity of the manufacturer(s) or the importer(s) or other
supplier as specified in Section 1.1 of Annex 6;
d.
A brief general description of the use(s), as specified in
Section 3.5 of Annex 6 , and of the conditions of use(s);
e.
Except where the downstream user is relying on the exemption in
Article 33(4)(c), a proposal for additional testing on
vertebrate animals, where this is considered necessary by the
downstream user to complete his chemical safety assessment.
2.
The downstream user shall update this information without delay in
the event of a change in the information reported in accordance
with paragraph 1.
3.
A downstream user shall report to the Ministry if his
classification of a substance is different to that of his
supplier.
4.
Except where a downstream user is relying on the exemption in
Article 33(4)(c), reporting in accordance with paragraphs 1 to 4
of this Article shall not be required in respect of a substance,
on its own or in a mixture, used by the downstream user in
quantities of less than one ton per year for that particular use.
Application of downstream user obligations
ARTICLE 35 – (1) Downstream users shall be required to comply with the
requirements of Article 33 at the latest 12 months after receiving a
registration number communicated to them by their suppliers in a
safety data sheet.
2.
Downstream users shall be required to comply with the requirements
of Article 34 at the latest six months after receiving a
registration number communicated to them by their suppliers in a
safety data sheet.
SIXTH PART
Evaluation
FIRST SECTION
Dossier Evaluation
Examination of testing proposals
ARTICLE 36 – (1) The Ministry shall examine any testing proposal set
out in a registration or a downstream user report for provision of the
information specified in Annexes 9 and 10 for a substance. Priority
shall be given to registrations of substances which have or may have
PBT, vPvB, sensitising and/or carcinogenic, mutagenic or toxic for
reproduction (CMR) properties, or substances above 100 tonnes per year
with uses resulting in widespread and diffuse exposure, provided they
fulfil the criteria for any of the following hazard classes or
categories set out in Annex 1 of Bylaw on Classification, Labelling
and Packaging of Substances and Mixtures.
a.
Hazard classes 2.1 to 2.4, 2.6 and 2.7, 2.8 types A and B, 2.9,
2.10, 2.12, 2.13 categories 1 and 2, 2.14 categories 1 and 2,
2.15 types A to F;
b.
Hazard classes 3.1 to 3.6, 3.7 adverse effects on sexual
function and fertility or on development, 3.8 effects other than
narcotic effects, 3.9 and 3.10;
c.
Hazard class 4.1;
ç) Hazard class 5.1.
2.
Information relating to testing proposals involving tests on
vertebrate animals shall be published on the Ministry website. The
Ministry shall publish on its website the name of the substance,
the hazard end-point for which vertebrate testing is proposed, and
the date by which any third party information is required. It
shall invite third parties to submit, using the format provided by
the Ministry, scientifically valid information and studies that
address the relevant substance and hazard end-point, addressed by
the testing proposal, within 45 days of the date of publication.
All such scientifically valid information and studies received
shall be taken into account by the Ministry in preparing its
decision in accordance with paragraph 3.
3.
On the basis of the examination under paragraph 1, the Ministry
shall draft one of the following decisions and that decision shall
be taken in accordance with the procedure laid down in Articles
43:
a.
A decision requiring the registrant(s) or downstream user(s)
concerned to carry out the proposed test and setting a deadline
for submission of the study summary, or the robust study summary
if required by Annex 1;
b.
A decision in accordance with subparagraph (a), but modifying
the conditions under which the test is to be carried out;
c.
A decision in accordance with subparagraphs (a), (b) or (ç) but
requiring registrant(s) or downstream user(s) to carry out one
or more additional tests in cases of non-compliance of the
testing proposal with Annexes 9, 10 and 11;
ç) A decision rejecting the testing proposal;
d.
A decision in accordance with subparagraphs (a), (b) or (c), if
several registrants or downstream users of the same substance
have submitted proposals for the same test, giving them the
opportunity to reach an agreement on who will perform the test
on behalf of all of them and to inform the Ministry accordingly
within 90 days. If the Ministry is not informed of such
agreement within 90 days, it shall designate one of the
registrants or downstream users, as appropriate, to perform the
test on behalf of all of them.
2.
The registrant or downstream user shall submit the information
required to the Ministry by the deadline set.
Compliance check of registrations
ARTICLE 37 – (1) The Ministry may examine any registration in order to
verify any of the following:
a.
That the information in the technical dossier(s) submitted
pursuant to Article 11 complies with the requirements of
Articles 11, 13 and 14 and with Annex 3, Annex 6, Annex 7, Annex
8, Annex 9 and Annex 10;
b.
That the adaptations of the standard information requirements
and the related justifications submitted in the technical
dossier(s) comply with the rules governing such adaptations set
out in Annexes 7 to 10 and with the general rules set out in
Annex 11;
c.
That any required chemical safety assessment and chemical safety
report comply with the requirements of Annex 1 and that the
proposed risk management measures are adequate;
ç) That any explanation(s) submitted in accordance with Article 12(3)
or Article 19(2) has an objective basis.
2.
On the basis of an examination made pursuant to paragraph 1, the
Ministry may, within 12 months of the start of the compliance
check, prepare a draft decision requiring the registrant(s) to
submit any information needed to bring the registration(s) into
compliance with the relevant information requirements and
specifying adequate time limits for the submission of further
information. Such a decision shall be taken in accordance with the
procedure laid down in Article 43.
3.
The registrant shall submit the information required to the
Ministry by the deadline set.
4.
To ensure that registration dossiers comply with this Bylaw, the
Ministry shall select a percentage of those dossiers, no lower
than 5 % of the total received by the Ministry for each tonnage
band, for compliance checking. The Ministry shall give priority,
but not exclusively, to dossiers meeting at least one of the
following criteria:
a.
The dossier contains information in Article 11(1)(a), (4), (6)
and/or (7) submitted separately as per Article 12(3); or
b.
The dossier is for a substance manufactured or imported in
quantities of one tonne or more per year and does not meet the
requirements of Annex 7 applying under either Article 13(1)(a)
or (b), as the case may be.
Check of information submitted and follow-up to dossier evaluation
ARTICLE 38 – (1) The Ministry shall examine any information submitted
in consequence of a decision taken under Articles 36 or 37, and draft
any appropriate decisions in accordance with these Articles, if
necessary.
2.
The Ministry shall use the information obtained from this
evaluation for the purposes of Article 40.
Procedure and time periods for examination of testing proposals
ARTICLE 39 –(1) The Ministry shall prepare the draft decisions in
accordance with the Article 36 (3) in order to fulfil the information
requirements in Annexes 9 and 10 by 31/12/2025 for the proposals
received by 31/12/2023 including the testing proposals.
SECOND SECTION
Substance Evaluation
Criteria for substance evaluation
ARTICLE 40 – (1) Prioritization shall be made by the Ministry on a
risk-based approach:
a.
Hazard information, for instance structural similarity of the
substance with known substances of concern or with substances
which are persistent and liable to bio-accumulate, suggesting
that the substance or one or more of its transformation products
has properties of concern or is persistent and liable to
bio-accumulate;
b.
Exposure information;
c.
Tonnage, including aggregated tonnage from the registrations
submitted by several registrants.
Requests for further information and check of information submitted
ARTICLE 41 – (1) Ministry may require further information from the
registrants defined in Annex 7, Annex 8, Annex 9 and Annex 10
including the ones not defined there.
2.
The registrant shall submit the information required to the
Ministry by the deadline set.
3.
The Ministry shall examine any information submitted, and shall
draft any appropriate decisions in accordance with this Article,
if necessary, within 12 months of the information being submitted.
2.
The Ministry shall finish its evaluation activities within 12
months of the start of the evaluation of the substance or within
12 months of the information being submitted under paragraph 2.
THIRD SECTION
Evaluation of Intermediates
Further information on on-site isolated intermediates
ARTICLE 42 – (1) For on-site isolated intermediates that are used in
strictly controlled conditions, neither dossier nor substance
evaluation shall apply. However, the Ministry considers that a risk to
human health or the environment, equivalent to the level of concern
arising from the use of substances meeting the criteria in Article 47,
arises from the use of an on-site isolated intermediate and that risk
is not properly controlled, it may:
a.
Require the registrant to submit a written justification on
further information directly related to the risk identified,
b.
Examine any information submitted and, if necessary, recommend
any appropriate risk reduction measures to address the risks
identified in relation to the site in question.
FOURTH SECTION
Common Provisions
Registrants' and downstream users' rights
ARTICLE 43 – (1) The Ministry shall notify any draft decision under
Articles 36, 37 or 41 to the registrant(s) or downstream user(s)
concerned, informing them of their right to comment within 30 days of
receipt. If the concerned registrant(s) or downstream user(s) wish to
comment, they shall provide their comments to the Ministry in 30 days.
The Ministry may amend the draft decision accordingly. In the case
that registrants and downstream users don’t notify their potential
comments to the Ministry in 30 days from the date of notification,
notification decision is deemed to be accepted.
2.
If a registrant has ceased the manufacture or import of the
substance, or the production or import of an article, or the
downstream user the use, he shall inform the Ministry of this fact
with the consequence that the registered volume in his
registration, if appropriate, shall be put to zero and no further
information may be requested with respect to that substance,
unless the registrant notifies the restart of the manufacture or
import of the substance or the production or import of the
article, or the downstream user notifies the restart of the use.
3.
The registrant may cease the manufacture or import of the
substance or the production or import of the article, or the
downstream user the use, upon receipt of the decision. In such
cases, the registrant, or downstream user, shall inform the
Ministry of this fact with the consequence that his registration,
or report, shall no longer be valid, and no further information
may be requested with respect to that substance, unless he submits
a new registration or report.
4.
The Ministry may request further information for the following(s)
in the context of Article 41:
a.
If a dossier has been prepared under Annex 15 and it was decided
to be harmful to the human or environmental health and so a
further information is needed;
b.
If the risk of exposure to the substance manufactured or imported
by the registrant or manufactured or imported in an article or
used by the downstream user is significantly increasing.
Cost sharing for tests without an agreement between registrants and/or
downstream users
ARTICLE 44 – (1) Where registrants or downstream users are required to
perform a test as a result of a decision taken under this Part, those
registrants or downstream users shall make every effort to reach an
agreement as to who is to carry it out on behalf of the other
registrants or downstream users and to inform the Ministry accordingly
within 90 days. If the Ministry is not informed of such agreement
within 90 days, it shall designate one of the registrants or
downstream users to perform the test on behalf of all of them.
2.
If a registrant or downstream user performs a test on behalf of
others, they shall all share the cost of that study equally.
3.
In the case referred to in paragraph 1, the registrant or
downstream user who performs the test shall provide each of the
others concerned with a copy of the full study report.
4.
The person performing and submitting the study shall have a claim
against the others accordingly. Any person concerned shall be able
to make a claim in order to prohibit another person from
manufacturing, importing or placing the substance on the market if
that other person either fails to pay his share of the cost or to
provide security for that amount or fails to hand over a copy of
the full study report of the study performed.
SEVENTH PART
Authorization
FIRST SECTION
Authorization Requirement
Authorization and Substitution
ARTICLE 45 – (1) All manufacturers, importers and downstream users
applying for authorizations shall analyse the availability of
alternatives and consider their risks, and the technical and economic
feasibility of substitution.
General provisions
ARTICLE 46 – (1) A manufacturer, importer or downstream user shall not
place a substance on the market for a use or use it himself if that
substance is included in Annex 14, unless:
a.
The use(s) of that substance on its own or in a mixture or the
incorporation of the substance into an article for which the
substance is placed on the market or for which he uses the
substance himself has been authorized in accordance with
Articles 50, 51, 52, 53, 54 or ;
b.
The use(s) of that substance on its own or in a mixture or the
incorporation of the substance into an article for which the
substance is placed on the market or for which he uses the
substance himself has been exempted from the authorization
requirement in Annex 14 itself in accordance with Article 48(2);
or
c.
The date referred to in Article 48(1)(c)(1) has not been
reached; or
ç) The date referred to in Article 48(1)(c)(1) has been reached and he
made an application 18 months before that date but a decision on the
application for authorization has not yet been taken; or
d.
In cases where the substance is placed on the market,
authorization for that use has been granted to his immediate
downstream user.
2.
A downstream user may use a substance meeting the criteria set out
in paragraph 1 provided that the use is in accordance with the
conditions of an authorization granted to an actor up his supply
chain for that use.
3.
Paragraphs 1 and 2 shall not apply to the use of substances in
scientific research and development. Annex 14 shall specify if
paragraphs 1 and 2 apply to product and process orientated
research and development as well as the maximum quantity exempted.
4.
Paragraphs 1 and 2 shall not apply to the following uses of
substances:
a.
Uses in plant protection products within the scope of Bylaw on the
Classification, Packaging and Labelling of Plant Protection
Products;
b.
Uses in biocidal products within the scope of Bylaw on Biocidal
Products;
c.
Use as motor fuels covered by Bylaw on Environmental Effects of
Motor Fuels and Diesel Fuels Types; published in the Official
Gazette dated 01/04/2017 and numbered 30025;
ç) Uses as fuel in mobile or fixed combustion plants of mineral oil
products and use as fuels in closed systems.
2.
In the case of substances that are subject to authorization only
because they meet the criteria in Article 47 (1) (a), (b) or (c)
or because they are identified in accordance with Article 47 (1)
(e) only because of hazards to human health, paragraphs 1 and 2 of
this Article shall not apply to the following uses:
a.
Uses in cosmetic products within the scope of Bylaw on Cosmetics ;
2.
Uses in food contact materials within the scope of Bylaw on the
Turkish Food Codex Substances and Materials in Contact with Food
Paragraphs 1 and 2 shall not apply to the use of substances when
they are present in mixtures:
a.
For substances referred to in Article 47 (1) (ç), (d) and (e),
below a concentration limit of 0,1 % weight by weight (w/w);
b.
For all other substances, below the lowest of the concentration
limits specified in Annex 6, Section 3 of Bylaw on Classification,
Labelling and Packaging of Substances and Mixtures which result in
the classification of the mixture as hazardous.
Substances to be included in Annex XIV
ARTICLE 47 – (1) The following substances defined as the substances of
high concern may be included in Annex 14 in accordance with the
procedure laid down in Article 48:
a.
Substances meeting the criteria for classification in the hazard
class carcinogenicity category 1A or 1B in accordance with title
3.6 of Annex 1 of Bylaw on Classification, Labelling and
Packaging of Substances and Mixtures;
b.
Substances meeting the criteria for classification in the hazard
class germ cell mutagenicity category 1A or 1B in accordance
with title 3.5 of Annex 1 of the Bylaw on Classification,
Labelling and Packaging of Substances and Mixtures ;
c.
Substances meeting the criteria for classification in the hazard
class reproductive toxicity category 1A or 1B in accordance with
title 3.7 of Annex 1 to Bylaw on Classification, Labelling and
Packaging of Substances and Mixtures;
ç) Substances which are persistent, bio accumulative and toxic in
accordance with the criteria set out in Annex 13 of this Bylaw;
d.
Substances which are very persistent and very bio accumulative
in accordance with the criteria set out in Annex 13 of this
Bylaw;
e.
SRechthoek 8 ubstances — such as those having endocrine
disrupting properties or those having persistent, bio
accumulative and toxic properties or very persistent and very
bio accumulative properties, which do not fulfill the criteria
of subparagraphs (ç) or (d) — for which there is scientific
evidence of probable serious effects to human health or the
environment which give rise to an equivalent level of concern to
those of other substances listed in this paragraph and which are
identified on a case-by-case basis in accordance with the
procedure set out in Article 49.
Inclusion of substances in Annex 14
ARTICLE 48 – (1) Whenever a decision is taken by the Ministry to
include the substances referred to in Article 47 in Annex 14, such a
decision shall specify for each substance:
a.
The identity of the substance as specified in Section 2 of Annex
6 ;
b.
The intrinsic property (properties) of the substance referred to
in Article 47;
c.
Transitional arrangements:
1.
The date(s) from which the placing on the market and the use
of the substance shall be prohibited unless an authorization
is granted, the sunset date, which should take into account,
where appropriate, the production cycle specified for that
use;
2.
A date or dates at least 18 months before the sunset date(s)
by which applications must be received if the applicant wishes
to continue to use the substance or place it on the market for
certain uses after the sunset date(s); these continued uses
shall be allowed after the sunset date until a decision on the
application for authorization is taken;
ç) Review periods for certain uses, if appropriate;
d.
Uses or categories of uses exempted from the authorization
requirement, if any, and conditions for such exemptions, if any.
2.
Uses or categories of uses may be exempted from the authorization
requirement provided that, on the basis of the existing specific
related legislation imposing minimum requirements relating to the
protection of human health or the environment for the use of the
substance, the risk is properly controlled. In the establishment
of such exemptions, account shall be taken, in particular, of the
proportionality of risk to human health and the environment
related to the nature of the substance, such as where the risk is
modified by the physical form.
3.
Prior to a decision to include substances in Annex 14, the
Ministry shall, determine priority substances to be included
specifying for each substance the items set out in paragraph 1.
Priority shall normally be given to substances with:
a.
PBT or vPvB properties; or
b.
Wide dispersive use; or
c.
High volumes.
The number of substances included in Annex 14 and the dates specified
under paragraph 1 shall also take account of the Ministry’s capacity
to handle applications in the time provided for.
2.
Before the Ministry adopts a decision it shall make it publicly
available on its website in accordance with Article 60 and 61,
clearly indicating the date of publicationand all interested
parties may submit comments within three months of the date of
publication, in particular on uses which should be exempt from the
authorization requirement. The Ministry shall make its decision
according to the received comments. In the event that the
substance proposed to be included in Annex 14 concerns the
Relevant Authorities other than the Ministry, the Ministry shall
first obtain the written opinion of such Relevant Authorities.
3.
Subject to paragraph 6, after inclusion of a substance in Annex
14, this substance shall not be subjected to new restrictions
under the procedure outlined in Part 8 covering the risks to human
health or the environment from the use of the substance on its
own, in a mixture or incorporation of a substance in an article
arising from the intrinsic properties specified in Annex 14.
4.
A substance listed in Annex 14 may be subjected to new
restrictions under the procedure outlined in Part 8 covering the
risks to human health or the environment from the presence of the
substance in (an) article(s).
5.
Substances for which all uses have been prohibited under Part 8 or
by other relevant legislation shall not be included in Annex 14 or
shall be removed from it.
6.
Substances which as a result of new information no longer meet the
criteria of Article 47 shall be removed from Annex 14 by the
Ministry.
Defining the substances in Article 47
ARTICLE 49- (1) The procedure mentioned in this article is applied in
order to define the substances compliant with the criteria mentioned
in Article 47 and the substances to be included in Annex 14.
(2) Before starting the procedures for the substances in Article 47,
the Ministry shall specify the substances in this Article in order to
prepare dossier under Annex 15 and announce that the dossier is
prepared under Annex 15 through website. The Ministry shall invite all
releted parties to send their opinions to the Ministry.
(3) Any Relevant Authority prepares a dossier for the substances for
which he thinks they are compliant with the criteria under Article 47
according to Annex 15 and send it to the Ministry. The Ministry shall
forward the dossier to the relevant entities within 30 days after
receiving if it is in accordance with Annex 15 .
(4) Beginning from the forward of the dossier within 60 days, all
relevant entities will send their comments to the Ministry.
(5) After the 60 day period mentioned in paragraph 4, , the Ministry
shall decide on adding or not the substance in paragraph 1 to the
list.
(6)After the decision on adding the substance, the Ministry shall
announce and update the list under paragraph 1 through website.
SECOND SECTION
Authorization
Granting of authorizations
ARTICLE 50 – (1) The Ministry shall be responsible for taking
decisions on applications for authorizations in accordance with this
Section.
2.
Without prejudice to paragraph 3 provisions of this Article an
authorization shall be granted if the risk to human health or the
environment from the use of a substance arising from the intrinsic
properties specified in Annex 14 is adequately controlled in
accordance with Section 6.4 of Annex 1 and as documented in the
applicant's chemical safety report. When granting the
authorization, and in any conditions imposed therein, the Ministry
shall take into account all discharges, emissions and losses,
including risks arising from diffuse or dispersive uses, known at
the time of the decision.
3.
Paragraph 2 shall not apply to:
a) Substances meeting the criteria in Article 47 (1) (a), (b), (c) or
(e) for which it is not possible to determine a threshold in
accordance with Section 6.4 of Annex 1;
b) Substances meeting the criteria in Article 47 (1) (ç) or (d);
c) Substances identified under Article 47 (1) (e) having persistent,
bio accumulative and toxic properties or very persistent and very bio
accumulative properties.
(4) If an authorisation cannot be granted under paragraph 2 or for
substances listed in paragraph 3, an authorisation may only be granted
if it is shown that socio-economic benefits outweigh the risk to human
health or the environment arising from the use of the substance and if
there are no suitable alternative substances or technologies. This
decision shall be taken after consideration of all of the following
elements and taking into account the opinions of the Risk Assessment
and the Socio-economic Analysis referred to in Article 54 (4)(a) and
(b):
a) The risk posed by the uses of the substance, including the
appropriateness and effectiveness of the risk management measures
proposed;
b) The socio-economic benefits arising from its use and the socio-
economic implications of a refusal to authorize as demonstrated by the
applicant or other interested parties;
c) the analysis of the alternatives submitted by the applicant under
Article 52(4)(d) or any substitution plan submitted by the applicant
under Article 52(4)(e), and any third party contributions submitted
under Article 54 (2);
ç) Available information on the risks to human health or the
environment of any alternative substances or technologies.
(5) When assessing whether suitable alternative substances or
technologies are available, all relevant aspects shall be taken into
account by the Ministry including:
a) Whether the transfer to alternatives would result in reduced
overall risks to human health and the environment, taking into account
the appropriateness and effectiveness of risk management measures;
b) The technical and economic feasibility of alternatives for the
applicant.
(6) A use shall not be authorized if this would constitute a
relaxation of a restriction set out in Annex 17.
(7) The authorization shall specify:
a) The person(s) to whom the authorization is granted;
b) The identity of the substance(s);
c) The use(s) for which the authorization is granted
ç) Any conditions under which the authorization is granted;
d) The time-limited review period;
e) Any monitoring arrangement.
(8) Notwithstanding any conditions of an authorization, the holder
shall ensure that the exposure is reduced to as low a level as is
technically and practically possible.
Review of authorizations
ARTICLE 51 – (1) Authorizations granted in accordance with Article 50
shall be regarded as valid until the Ministry decides to amend or
withdraw the authorization in the context of a review, provided that
the holder of the authorization submits a review report at least 18
months before the expiry of the time-limited review period. Rather
than re-submitting all elements of the original application for the
current authorization, the holder of an authorization may submit only
the number of the current authorization, subject to the second, third
and fourth subparagraphs.
A holder of an authorization granted in accordance with Article 50
shall submit an update of the analysis of alternatives referred to in
Article 52(4)(d), including information about any relevant research
and development activities by the applicant, if appropriate, and any
substitution plan submitted under Article 52(4)(e). If the update of
the analysis of alternatives shows that there is a suitable
alternative available taking into account the elements in Article
50(5), he shall submit a substitution plan, including a timetable for
proposed actions by the applicant. If the holder cannot demonstrate
that the risk is adequately controlled, he shall also submit an update
of the socio- economic analysis contained in the original application.
If he can now demonstrate that the risk is adequately controlled, he
shall submit an update of the chemical safety report.
If any other elements of the original application have changed, he
shall also submit updates of these element(s).
When any updated information is submitted in accordance with this
paragraph, any decision to amend or withdraw the authorization in the
context of the review shall be taken in accordance with the procedure
referred to in Article 54 applied mutatis mutandis.
2.
The Ministry shall set a reasonable deadline by which the
holder(s) of the authorization may submit further information
necessary for the review and indicate by when it will take a
decision in accordance with Article 54. Authorizations may be
reviewed at any time if:
a.
The circumstances of the original authorization have changed so
as to affect the risk to human health or the environment, or the
socio- economic impact; or
b.
New information on possible substitutes becomes available.
2.
In its review decision the Ministry may, if circumstances have
changed and taking into account the principle of proportionality,
amend or withdraw the authorization, if under the changed
circumstances it would not have been granted or if suitable
alternatives in accordance with Article 50(5) become available. In
the latter case the Ministry shall require the holder of the
authorization to present a substitution plan if he has not already
done so as part of his application or update.
In cases where there is a serious and immediate risk for human health
or the environment, the Ministry may suspend the authorization pending
the review, taking into account the principle of proportionality.
2.
If an environmental quality standard referred to in relevant
legislation on IPPC is not met, the authorizations granted for the
use of the substance concerned may be reviewed.
3.
If the environmental objectives as referred to in Article 4 of
Bylaw on Water Pollution Control published in Official Gazette
dated 31/12/2004 and numbered 25687 are not met, the
authorizations granted for the use of the substance concerned in
the relevant river basin may be reviewed.
4.
If a use of a substance is subsequently prohibited or otherwise
restricted in regulations on persistent organic pollutants, the
Ministry shall withdraw the authorization for that use.
Applications for authorizations
ARTICLE 52 – (1) An application for an authorization shall be made to
the Ministry through Chemicals Registration System in the website of
Ministry.
2.
Applications for authorization may be made by the manufacturer(s),
importer(s) and/or downstream user(s) of the substance.
Applications may be made by one or several persons.
3.
Applications may be made for one or several substances that meet
the definition of a group of substances in Section 1.5 of Annex
11, and for one or several uses. Applications may be made for the
applicant's own use(s) and/or for uses for which he intends to
place the substance on the market.
4.
An application for authorization shall include the following
information:
a.
The identity of the substance(s), as referred to in Section 2 of
Annex 6 ;
b.
The name and contact details of the person or persons making the
application;
c.
A request for authorization, specifying for which use(s) the
authorization is sought;
ç) Unless already submitted as part of the registration, a chemical
safety report in accordance with Annex 1 covering the risks to human
health and/or the environment from the use of the substance(s) arising
from the intrinsic properties specified in Annex 14;
d.
An analysis of the alternatives considering their risks and the
technical and economic feasibility of substitution and
including, if appropriate information about any relevant
research and development activities by the applicant;
e.
Where the analysis referred to in paragraph (d) shows that
suitable alternatives are available, taking into account the
elements in Article 50(5), a substitution plan including a
timetable for proposed actions by the applicant.
2.
The application may include:
a.
A socio-economic analysis conducted in accordance with Annex 16;
b.
A justification for not considering risks to human health and
the environment arising either from:
1.
Emissions of a substance from an installation for which a
permit was granted; or
2.
Discharges of a substance from a point source governed by the
requirement for prior regulation.
2.
The application shall not include the risks to human health
arising from the use of a substance in a medical device in the
scope of Bylaw on Medical Devices published in the Official
Gazette dated 07/06/2011 and numbered 27957, Bylaw on Invasive
Active Medical Devices published in the Official Gazette dated
07/06/2011 and numbered 27957 and Bylaw on Medical Diagnosis
Devices Which Are Used Outside The Body (In vitro) published in
the Official Gazette dated 09/01/2007 and numbered 26398.
Subsequent applications for authorization
ARTICLE 53 – (1) If an application has been made for a use of a
substance, a subsequent applicant may refer to the appropriate parts
of the previous application submitted in accordance with Article
52(4)(ç), (d), (e) and (5)(a), provided that the subsequent applicant
has permission from the previous applicant to refer to these parts of
the application.
2.
If an authorization has been granted for a use of a substance, a
subsequent applicant may refer to the appropriate parts of the
previous application submitted in accordance with Article
52(4)(ç), (d) and (e) and (5)(a), provided that the subsequent
applicant has permission from the holder of the authorization to
refer to these parts of the application.
3.
Before referring to any previous application in accordance with
paragraphs 1 and 2, the subsequent applicant shall update the
information of the original application as necessary.
Procedure for authorization
ARTICLE 54 – (1) The Ministry shall acknowledge the date of receipt of
the application. Following the receipt of application, the Ministry
shall conduct the Risk Assessment and Socio-economic Analysis referred
to in this Article and shall give its draft opinions within ten months
of the date of receipt of the application.
2.
The Ministry shall make available on its website broad information
on uses, taking into account Articles 60 and 61 on access to
information, for which applications have been received and for
reviews of authorizations, with a deadline by which information on
alternative substances or technologies may be submitted by
interested third parties.
3.
During the process for adoption of authorization decisions in
paragraph 1, the Ministry shall first check that the application
includes all the information specified in Article 52 that is
relevant to its remit. If necessary, the Ministry shall, request
to the applicant for additional information to bring the
application into conformity with the requirements of Article 52.
The Ministry may, if it deems it necessary, require the applicant
or request third parties to submit, within a specified time
period, additional information on possible alternative substances
or technologies. The Ministry shall also take into account any
information submitted by third parties.
4.
The draft opinions shall include the following elements:
a.
Risk Assessment: an assessment of the risk to human health
and/or the environment arising from the use(s) of the substance,
including the appropriateness and effectiveness of the risk
management measures as described in the application and, if
relevant, an assessment of the risks arising from possible
alternatives;
b.
Socio-economic Analysis: an assessment of the socio-economic
factors and the availability, suitability and technical
feasibility of alternatives associated with the use(s) of the
substance as described in the application, when an application
is made in accordance with Article 52 and of any third party
contributions submitted under paragraph 2 of this Article.
(5) The Ministry shall send these draft opinions to the applicant by
the end of the deadline set out in paragraph 1. Within 60 days of
receipt of the draft opinion, the applicant may provide written notice
that he wishes to comment.
If the applicant does not send comment to the Ministry in 60 days, the
draft opinion will be finalized. After the Ministry takes the written
opinion in 60 days, it will finalize its draft opinion in 60 days.
(6) The Ministry shall determine which parts of its opinions and parts
of any attachments thereto should be made publicly available on its
website.
(7) In cases covered by Article 53(1), the Ministry shall treat the
applications together, provided the deadlines for the first
application can be met.
(8) The Ministry shall prepare a draft authorization decision within
90 days of the issuance of its opinions. A final decision granting or
refusing the authorization shall be taken.
(9) Summaries of the Ministry decisions, including the authorization
number and the reasons for the decision, in particular where suitable
alternatives exist, shall be published in the web-site of the
Ministry.
(10) In cases covered by Article 53(2), the deadline set out in
paragraph 1 of this Article shall be shortened to five months.
THIRD SECTION
Authorizations in the Supply Chain
Obligation of holders of authorizations
ARTICLE 55 – (1) Holders of an authorization, as well as downstream
users referred to in Article 46(2) including the substances in a
mixture, shall include the authorization number on the label before
they place the substance or a mixture containing the substance on the
market for an authorised use without prejudice to Bylaw on the
Classification, Labelling and Packaging of Substances and Mixtures.
Downstream users
ARTICLE 56 – (1) Downstream users using a substance in accordance with
Article 46(2) shall notify the Ministry within 90 days of the first
supply of the substance.
2.
The Ministry shall establish and keep up to date a register of
downstream users who have made a notification in accordance with
paragraph 1.
EIGHTH PART
Restrictions on the Manufacturing, Placing on the Market and Use of
Certain Hazardous Substances, Mixtures and Articles
FIRST SECTION
Restrictions
Placing Restriction
ARTICLE 57 – (1) A substance on its own, in a mixture or in an
article, for which Annex 17 contains a restriction shall not be
manufactured, placed on the market or used unless it complies with the
conditions of that restriction. This shall not apply to the
manufacture, placing on the market or use of a substance in scientific
research and development. Annex 17 shall specify if the restriction
shall not apply to product and process orientated research and
development, as well as the maximum quantity exempted.
2.
Paragraph 1 shall not apply to the use of substances in cosmetic
products, as defined by Bylaw on Cosmetics with regard to
restrictions addressing the risks to human health within the scope
of that Bylaw.
SECOND SECTION
Restrictions Process
Introducing new and amending current restrictions
ARTICLE 58 – (1) When there is an unacceptable risk to human health or
the environment, arising from the manufacture, use or placing on the
market of substances, Annex 17 shall be amended by the Ministry by
adopting new restrictions, or amending current restrictions in Annex
17, for the manufacture, use or placing on the market of substances on
their own, in mixtures or in articles. Any amendment shall take into
account the socio- economic impact of the restriction, including the
availability of alternatives.
2.
The first subparagraph shall not apply to the use of a substance
as an on-site isolated intermediate.
3.
Ministry shall conduct risk assessment and socio-economic analysis
to evaluate the risk to human health or the environment and the
socio-economic impact of restriction during the restriction
process. Ministry may use the services of third parties or compose
committees consisting of experts in order to conduct or help to
conduct such Risk Assessments and socio-economic analysis.
4.
Any relevant entity may prepare a restriction proposal dossier
under Annex 15 and can submit this to the Ministry.
NINETH PART
Fees
FIRST SECTION
Circulation Capital Costs
Circulation capital costs
ARTICLE 59 – (1) The processes in the scope of Article 7(1), Article
8(1) and (5), Article 10(2), Article 12, Article 17(2), Article 18(2),
Article 19, Article 22(1), Article 51, Article 52 and Article 61(2)
are subject to fees.
(2) The fees that shall be paid in the scope of this Bylaw, is
determined annually and published at the website of the Ministry in
the circulating capital enterprise unit price list.
(3) No fee shall be taken for the substances in the 1-10 tonnage band
which have all of the information according to Annex 7 in their
registration dossier.
TENTH PART
Information
FIRST SECTION
Access to Information
Access to information
ARTICLE 60– (1) Disclosure of the following information shall normally
be deemed to undermine the protection of the commercial interests of
the concerned person:
a) details of the full composition of a mixture ;
b) without prejudice to Article 8(6) and Article 54 (2), the precise
use, function or application of a substance or mixture , including
information about its precise use as an intermediate;
c) the precise tonnage of the substance or mixture manufactured or
placed on the market;
ç) links between a manufacturer or importer and his distributors or
downstream users.
(2)Where urgent action is essential to protect human health, safety or
the environment, such as emergency situations, the Ministry may
disclose the information referred to in this paragraph.
Public access
ARTICLE 61 – (1) The following information held by the Ministry on
substances whether on their own, in mixtures or in articles, shall be
made publicly available, free of charge, over the Internet:
a.
Without prejudice to paragraph 2(e) of this Article, the name
in the IUPAC nomenclature for substances fulfilling the
criteria for any of the following hazard classes or categories
set out in Annex 1 to Bylaw on the Classification, Labelling
and Packaging of Substances and Mixtures
1) Hazard classes 2.1 to 2.4, 2.6 and 2.7, 2.8 types A and B, 2.9,
2.10, 2.12, 2.13 categories 1 and 2, 2.14 categories 1 and 2, 2.15
types A to F;
2) Hazard classes 3.1 to 3.6, 3.7 adverse effects on sexual function
and fertility or on development, 3.8 effects other than narcotic
effects, 3.9 and 3.10;
3) Hazard class 4.1;
4) Hazard class 5.1;
b) If applicable, the name of the substance as given in EINECS;
c) The classification and labelling of the substance;
ç) Physicochemical data concerning the substance and on pathways and
environmental fate;
d) toxicological and eco toxicological information;
e) Any derived no-effect level (DNEL) or predicted no-effect
concentration (PNEC);
f) The guidance on safe use provided in accordance with Sections 4 and
5 of Annex 6 ;
g) Analytical methods if requested in accordance with Annexes 9 or 10
which make it possible to detect a dangerous substance when discharged
into the environment as well as to determine the direct exposure of
humans.
2.
The following information on substances whether on their own, in
mixtures or in articles, shall be made publicly available, free of
charge, over the Internet except where a party submitting the
information submits a justification in accordance with Article
11(a)(11), accepted as valid by the Ministry, as to why such
publication is potentially harmful for the commercial interests of
the registrant or any other party concerned:
a.
If essential to classification and labelling, the degree of purity
of the substance and the identity of impurities and/or additives
which are known to be hazardous;
b.
The total tonnage band (i.e. 1 to 10 tons, 10 to 100 tons, 100 to
1 000 tons or over 1 000 tons) within which a particular substance
has been registered;
c) The study summaries or robust study summaries of the information
referred to in paragraph 1(ç) and (d);
ç) Information, other than that listed in paragraph 1, contained in
the safety data sheet;
d) The trade name(s) of the substance;
e) Subject to Article 26 of Bylaw on the Classification, Labelling and
Packaging of Substances and Mixtures , the name in the IUPAC
nomenclature for substances that are only used as one or more of the
following:
1.
As an intermediate;
2.
In scientific research and development
3.
In product and process orientated research and development.
ELEVENTH PART
Inspectıon and Enforcement
FIRST SECTION
Inspectıon and Enforcement
Inspection
ARTICLE 62 – (1) Of this Bylaw:
a.
Inspections regarding Article 46 and 57 shall be conducted
according to the Law numbered 4703, Law on Occupational Health and
Safety published in the Official Gazette dated 13/07/2012 and
numbered 6331, Law on Provincial Administration published in the
Official Gazette dated 10/06/1949 and numbered 5442 and Law
numbered 5996 by Relevant Institutions.
b.
Inspections regarding the other provisions shall be conducted
according to Law numbered 2872 and Law numbered 4703 by the
Ministry.
.
Enforcement
ARTICLE 63 – (1) In case the breech of the provisions of this Bylaw,
enforcement and penalties indicated in Article 12 ,13 and (20)(1) (y)
of Law numbered 2872, Article 11 and 12 of Law numbered 4703, Articles
36 to 42 of Law numbered 5996 and Article 66 of Law numbered 5442
shall be applied.
TWELVETH PART
Miscellaneous and Final Provisions
FIRST SECTION
Miscellaneous Provisions
Repeals
ARTICLE 64 – (1) Following Bylaws shall be repealed upon the entry
into force of this Bylaw:
a) Bylaw on Safety Data Sheets Concerning Hazardous Substances and
Mixtures published in the Turkish Official Gazette dated 13/12/ 2014
numbered 29204
b) Bylaw on Inventory and Control of Chemicals published in the
Turkish Official Gazette dated 26/12/ 2008 numbered27092 (bis)
c) Bylaw on Restriction and Ban of Hazardous Substances and Mixtures
published in the Official Gazette dated 26/12/ 2008 numbered 27092
(bis)
Harmonisation of European Union Legislation
Madde 65- (1) This Bylaw was prepared taking into account Regulation
of European Parliament and Council numbered 1907/2006/EC on
Registration, Evaluation, Authorization and Restriction of Chemicals
in the framework of harmonization of European Union acquie.
Transitional provision
TRANSITIONAL ARTICLE 1- (1) All registrants, shall send a pre-SIEF
including below mentioned information to the Ministry through
Chemicals Registration System in the website of Ministry until
31/12/2020:
a) substance identity according to Annex-6;
b) Role in the supply chain
TRANSITIONAL ARTICLE 2- (1) If substances on their own or in a mixture
are manufactured or imported before 31/12/2023 and equal to or more
than 1tonne/year, Articles 7 and/or 8 or 17 or 18 are executed between
dates 31/12/2020 and 31/12/2023.
(2) Safety Data Sheets shall be prepared according to the Bylaw on
Safety Data Sheets Concerning Hazardous Substances and Mixtures until
31/12/2023.
(3) Safety Data Sheets can be prepared according to this Bylaw from
the execution date of Article 27 until 31/12/2023. In these cases,
provisions of Bylaw on Safety Data Sheets Concerning Hazardous
Substances and Mixtures will not be applied.
(4) Chemicals Assessment Specialist can prepare a safety data sheet
also according to the Bylaw on Safety Data Sheets Concerning Hazardous
Substances and Mixtures.
Entry into Force
ARTICLE 66- (1) Of this Bylaw;
a) Articles 6, 40-56 will enter into force on 31/12/2023,
b) Article 57(1);
(1) Entries 28, 29, 30, 31, 32, 34, 35, 36, 37, 38, 40, 41, 45, 48,49,
54, 55,57, 58, 60 of Annex 17 will enter into force on 31/12/2018,
(2) Entry 62 of Annex 17 will enter into force on 31/12/2019
(3) Entries 46a, paragraphs 1 to 4 of 47 and 65 of Annex 17 will enter
into force on 31/12/2021
(4) Enty 66 of Annex 17 will enter into force on 31/12/2022
(5) All other entries of Annex 17 will enter into force 6 months later
the date of its publication on the Official Gazette.
c) Article 64(1)(a) will enter into force on 31/12/2023, Article
64(1)(b) will enter into force on the published day,
ç) All other provisions will enter into force 6 months later the date
of its publication on the Official Gazette.
Execution
ARTICLE 67 – (1) Of this Bylaw;
a.
Article 58 (1) shall be executed by the Minister of
Environment and Urbanization and Minister of Health jointly.
b.
Other provisions shall be executed by the Minister of
Environment and Urbanization.
38

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