The REACH etc. (Amendment) Regulations 2021
The requirements of paragraph 3(2) of Schedule 7 to that Act (relating to the appropriate Parliamentary procedure for these Regulations) have been satisfied.
PART 1Introductory
Citation and commencement1.
(1)
These Regulations may be cited as the REACH etc. (Amendment) Regulations 2021.
(2)
These Regulations come into force on 30th September 2021.
PART 2Amendment of Regulation (EC) No 1907/2006
Amendment of Regulation (EC) No 1907/20062.
Article 33.
“44.
relevant medical device: means a medical device within the scope of—
(a)
the Medical Devices Regulations 20023;(b)
Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices4 as it has effect in EU law; or(c)
Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices5 as it has effect in EU law;45.
relevant accessory to a medical device: means an accessory to a medical device within the scope of—
(a)
the Medical Devices Regulations 2002;
(b)
Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices as it has effect in EU law; or
(c)
Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices as it has effect in EU law.”
Article 604.
Article 625.
Annex 126.
In Annex 12 (general provisions for downstream users to assess substances and prepare chemical safety reports), in the introduction, in the fifth paragraph, for “Community” substitute “other”.
Annex 147.
(1)
In Annex 14 (list of substances subject to authorisation), entry 42 (4-(1, 1, 3, 3-Tetramethylbutyl)phenol, ethoxylated (covering well-defined substances and UVCB substances, polymers and homologues)) is amended in accordance with this regulation.
(2)
In the entry for the column headed “latest application date”, in point (b)—
(a)
in the first indent—
(i)
(ii)
before “medical devices”, in the first place that it occurs, insert “relevant”,
(iii)
before “accessories” insert “relevant”,
(iv)
omit the words from “falling within” to “of the Council,”;
(b)
in the second indent—
(i)
before “medical devices”, in the first place that it occurs, insert “relevant”,
(ii)
before “accessories” insert “relevant”,
(iii)
omit the words from “falling within” to “2017/746,”.
(3)
In the entry for the column headed “sunset date”, in point (b)—
(a)
in the first indent—
(i)
for “Directive 2001/83/EC” substitute “the Human Medicines Regulations 2012”,
(ii)
before “medical devices”, in the first place that it occurs, insert “relevant”,
(iii)
before “accessories” insert “relevant”,
(iv)
omit the words from “falling within” to “2017/746,”;
(b)
in the second indent—
(i)
before “medical devices”, in the first place that it occurs, insert “relevant”,
(ii)
before “accessories” insert “relevant”,
(iii)
omit the words from “falling within” to “2017/746,”.
Annex 178.
(1)
Annex 17 (restrictions on the manufacture, placing on the market and use of certain dangerous substances, mixtures and articles) is amended in accordance with this regulation.
(2)
(a)
before “medical devices” insert “relevant”;
(b)
omit “within the scope of the Medical Devices Regulations 2002”.
(3)
(a)
in paragraph 3(c)—
(i)
after “2032 to” insert “relevant”,
(ii)
omit “within the scope of the Medical Devices Regulations 2002”;
(b)
in paragraph 4(d)(i)—
(i)
after “implantable” insert “relevant”,
(ii)
omit “within the scope of the Medical Devices Regulations 2002”;
(c)
in paragraph 6(b), after “implantable” insert “relevant”.
(4)
(5)
In entry 74 (diisocyanates etc.), in the second column—
(a)
“6.
The training:
(a)
must comply with any other requirements contained in any other legislation that relate to the delivery of the training elements referred to in paragraph 5, and
(b)
is in addition to any other training required by any other legislation.”;
(b)
in paragraph 7, omit the words from “in the official” to the end of the first sentence;
(c)
in paragraph 9, in the opening text—
(i)
for “Member States” substitute “The Agency”,
(ii)
for “their reports” substitute “its report”,
(iii)
for “117(1)” substitute “117(2)”;
(d)
in paragraph 9, omit subparagraphs (a) and (c);
(e)
in paragraph 10, omit “Union”.
PART 3Amendment of Implementing Regulations
Commission Implementing Regulation (EU) 2019/16929.
(1)
(2)
In Article 3, after “Article 29 of Regulation 1907/2006” insert “as it has effect in EU law”.
(3)
Omit Article 4(1).
(4)
In Article 4(2)—
(a)
omit “pre-registrations made in accordance with Article 28 of Regulation (EC) No 1907/2006 shall no longer be valid and”;
(b)
after “and 27” insert “of Regulation (EC) No 1907/2006”.
(5)
Omit Article 5.
Commission Implementing Regulation (EU) 2020/143510.
(1)
(2)
In Article 6(1), for “Annex VI to Regulation (EC) No 1272/2008 of the European Parliament and of the Council” substitute “the GB mandatory classification and labelling list”.
PART 4Amendment of Implementing Decisions
Commission Implementing Decision C(2019) 501811.
(1)
(2)
In Article 2(3), for “competent authority of the Member State” substitute “Agency (as defined in Article 2A of Regulation (EC) No 1907/2006)”.
(3)
In Article 2(9), for “competent authority of the Member State where the authorised use takes place” substitute “Agency”.
(4)
In Article 3(3), for “competent authority of the Member State” substitute “Agency”.
(5)
In Article 3(11), for “competent authority of the Member State where the authorised use takes place” substitute “Agency”.
(6)
In Article 6(5), for “competent authority of the Member State where the authorised use takes place” substitute “Agency”.
(7)
In Article 8—
(a)
for “competent authority of the Member State where the authorised use takes place” substitute “Agency”;
(b)
omit “in an official language of that Member State”.
Commission Implementing Decision C(2019) 502312.
(1)
(2)
In the first subparagraph of Article 2(2)(a), for “competent authority” substitute “Agency (as defined in Article 2A of Regulation (EC) No 1907/2006)”.
(3)
In Article 3(6), for “competent authority of the Member State where the use takes place” substitute “Agency”.
(4)
In Article 3(7), for “competent authority of the Member State where the authorised use takes place” substitute “Agency”.
(5)
In Article 3(10), for “competent authorities of the Member State where the use takes place” substitute “Agency”.
(6)
In Article 6, for the words from “competent authority of the Member State” to the end substitute “Agency”.
Commission Implementing Decision C(2019) 744713.
(1)
(2)
In Article 2(3), for “competent authorities” substitute “Agency (as defined in Article 2A of Regulation (EC) No 1907/2006)”.
(3)
In Article 2(7), for “competent authorities of the Member States where an authorised use takes place” substitute “Agency”.
(4)
In the second subparagraph of Article 2(8), for “competent authorities of Member States” substitute “Agency”.
(5)
In Article 2(12), for “competent authorities of the Member State where the authorised uses take place” substitute “Agency”.
(6)
In Article 2(14), for “competent authorities of the Member State where the authorised uses take place” substitute “Agency”.
(7)
In Article 2(15), for “competent authority of the Member State where the use takes place” substitute “Agency”.
(8)
In Article 7—
(a)
for “competent authority of the Member States where the authorised uses take place” substitute “Agency”;
(b)
for “competent authority of the Member State where the authorised use takes place in an official language of that Member State” substitute “Agency”.
Commission Implementing Decision C(2019) 744814.
(1)
(2)
In Article 2(4), for “competent authority of the Member State where the authorised use takes place” substitute “Agency (as defined in Article 2A of Regulation (EC) No 1907/2006)”.
(3)
In Article 2(9), for “national competent authorities” substitute “the Agency”.
(4)
In Article 2(11), for “competent authorities of the Member State where the authorised uses take place” substitute “Agency”.
(5)
In Article 2(13), for “competent authority of the Member State where the authorised use takes place” substitute “Agency”.
(6)
In Article 2(14), for “competent authority of the Member State where the use takes place” substitute “Agency”.
(7)
In Article 6, for the words from “competent authority” to the end substitute “Agency”.
Commission Implementing Decision C(2019) 768315.
(1)
(2)
In Article 2(2), for “competent authorities” substitute “Agency (as defined in Article 2A of Regulation (EC) No 1907/2006)”.
(3)
In Article 2(4), for “competent authorities of the Member State where the authorised use takes place” substitute “Agency”.
(4)
In Article 2(8), for “national competent authorities” substitute “the Agency”.
(5)
In Article 2(11), for “competent authorities of the Member State where the authorised uses take place” substitute “Agency”.
(6)
In Article 2(13), for “competent authorities of the Member State where the authorised use takes place” substitute “Agency”.
(7)
In Article 2(14), for “competent authority of the Member State where the use takes place” substitute “Agency”.
(8)
In Article 6—
(a)
for “competent authority of the Member State where the authorised use takes place” substitute “Agency”;
(b)
omit “in an official language of that Member State”.
Commission Implementing Decision C(2020) 205616.
(1)
(2)
In Article 2(2), in the second subparagraph, for “competent authorities” substitute “Agency (as defined in Article 2A of Regulation (EC) No 1907/2006)”.
(3)
In Article 2(5), for the words from “competent authority” to the end substitute “Agency”.
(4)
In Article 2(6), in the second subparagraph, for the words from “competent authority” to the end substitute “Agency”.
(5)
In Article 2(12), for “competent authorities of the Member State where the use takes place” substitute “Agency”.
(6)
In Article 2(14), for the words from “competent authorities” to the end substitute “Agency”.
(7)
In Article 2(17), for “competent authority of the Member State where the use takes place” substitute “Agency”.
(8)
In Article 5(b), omit “Agency’s”.
(9)
In Article 6, for the words from “competent authority” to the end substitute “Agency”.
Commission Implementing Decision C(2020) 207317.
(1)
(2)
In Article 2(2), in the second subparagraph, for “competent authorities of the Member State where the authorised use takes place” substitute “Agency (as defined in Article 2A of Regulation (EC) No 1907/2006)”.
(3)
In Article 2(5), for the words from “competent authority” to the end substitute “Agency”.
(4)
In Article 2(7), for the words from “competent authority” to the end substitute “Agency”.
(5)
In Article 2(14), for “competent authority of the Member State where the use takes place” substitute “Agency”.
(6)
In Article 7, for the words from “competent authority” to the end substitute “Agency”.
Commission Implementing Decision C(2020) 207618.
(1)
(2)
In Article 2(2), in the third subparagraph, for “competent authorities” substitute “Agency (as defined in Article 2A of Regulation (EC) No 1907/2006)”.
(3)
In Article 2(5), for the words from “competent authorities” to the end substitute “Agency”.
(4)
In Article 2(6), in the second subparagraph, for the words from “competent authority” to the end substitute “Agency”.
(5)
In Article 2(9), for the words from “competent authorities” to the end substitute “Agency”.
(6)
In Article 2(12), for “competent authority of the Member State where the use takes place” substitute “Agency”.
(7)
In Article 7, for the words from “competent authority” to the end substitute “Agency”.
Commission Implementing Decision C(2020) 208419.
(1)
(2)
In Article 2(2), in the third subparagraph, for “competent authorities” substitute “Agency (as defined in Article 2A of Regulation (EC) No 1907/2006)”.
(3)
In Article 2(5), for the words from “competent authorities” to the end substitute “Agency”.
(4)
In Article 2(6), in the second subparagraph, for the words from “competent authority” to the end substitute “Agency”.
(5)
In Article 2(10), for the words from “competent authorities” to the end substitute “Agency”.
(6)
In Article 2(13), for “competent authority of the Member State where the use takes place” substitute “Agency”.
(7)
In Article 4(2), in the second subparagraph, for the words from “competent authority” to the end substitute “Agency”.
(8)
In Article 4(4), for “competent authority of the Member State where the authorised use takes place” substitute “Agency”.
(9)
In Article 6(3), for the words from “competent authorities” to the end substitute “Agency”.
(10)
In Article 6(6), for “competent authority of the Member State where the use takes place” substitute “Agency”.
(11)
In Article 8, for the words from “competent authority” to the end substitute “Agency”.
Commission Implementing Decision C(2020) 208920.
(1)
(2)
In Article 2(2), in the third subparagraph, for the words from “competent authorities” to the end substitute “Agency (as defined in Article 2A of Regulation (EC) No 1907/2006)”.
(3)
In Article 2(5), for the words from “competent authorities” to the end substitute “Agency”.
(4)
In Article 2(6), in the second subparagraph, for the words from “competent authorities” to the end substitute “Agency”.
(5)
In Article 2(10), for the words from “competent authorities” to the end substitute “Agency”.
(6)
In Article 2(13), for “competent authority of the Member State where the uses take place” substitute “Agency”.
(7)
In Article 7, for the words from “competent authority” to the end substitute “Agency”.
Commission Implementing Decision C(2020) 623121.
(1)
(2)
In Article 2(2), in the second subparagraph, for “competent authorities” substitute “Agency”.
(3)
In Article 2(5), for the words from “competent authority” to the end substitute “Agency”.
(4)
In Article 2(6), for “competent authority of the Member States” substitute “Agency”.
(5)
In Article 2(10), for “competent authorities of the Member States where the use takes place” substitute “Agency”.
(6)
In Article 2(12), for the words from “competent authorities” to the end substitute “Agency”.
(7)
In Article 2(15), for “competent authority of the Member State where the use takes place” substitute “Agency”.
(8)
In Article 5(b), omit “Agency’s”.
(9)
In Article 6, for the words from “competent authority” to the end substitute “Agency”.
Commission Implementing Decision C(2020) 651822.
(1)
(2)
In Article 2(2), in the second subparagraph, for “competent authorities” substitute “Agency (as defined in Article 2A of Regulation (EC) No 1907/2006)”.
(3)
In Article 2(5), for the words from “competent authority” to the end substitute “Agency”.
(4)
In Article 2(12), for the words from “competent authorities” to the end substitute “Agency”.
(5)
In Article 2(15), for “competent authority of the Member State where the use takes place” substitute “Agency”.
(6)
In Article 6, for the words from “competent authority” to the end substitute “Agency”.
Commission Implementing Decision C(2020) 879723.
(1)
(2)
In Article 2(2), in the second subparagraph, for “competent authorities of the Member State where an authorised use takes place” substitute “Agency (as defined in Article 2A of Regulation (EC) No 1907/2006)”.
(3)
In Article 2(5), for “competent authorities of the Member States where the authorised uses take place” substitute “Agency”.
(4)
In Article 2(7), for the words from “competent authorities” to the end substitute “Agency”.
(5)
In Article 6(2), for the words from “competent authorities” to the end substitute “Agency”.
(6)
In Article 8(5), for the words from “competent authorities” to the end substitute “Agency”.
(7)
In Article 10, for the words from “competent authority” to the end substitute “Agency”.
These Regulations are made in exercise of the powers conferred by section 8(1) of the European Union (Withdrawal) Act 2018 (c. 16) in order to address failures of retained EU law to operate effectively and other deficiencies (in particular under section 8(2)(a) to (d) and (g)) arising from the withdrawal of the United Kingdom from the European Union.
Part 2 of these Regulations amends the retained version of Regulation (EC) No 1907/2006 of the European Parliament and of the Council concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH).
Part 3 of these Regulations amends the retained versions of two Commission Implementing Regulations made under Regulation (EC) No 1907/2006. Regulation 9 amends Regulation (EU) 2019/1692 relating to the application of certain registration and data-sharing provisions. Regulation 10 amends Regulation (EU) 2020/1435 relating to registrants’ duties to update their registrations.
Part 4 of these Regulations amends a number of Commission Implementing Decisions that granted authorisations under Regulation (EC) No 1907/2006 before the end of the transition period.
An impact assessment has not been produced for this instrument as no, or no significant, impact on the private, voluntary or public sector is foreseen.