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Amendments to retained EU lawU.K.

2.—(1) Schedule 1 contains amendments to the following subordinate legislation—

(a)the Health and Safety (Enforcing Authority) Regulations 1998 M1;

F1(b). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(c)the Control of Substances Hazardous to Health Regulations 2002 M2;

(d)the Dangerous Substances and Explosive Atmospheres Regulations 2002 M3;

F2(e). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

F3(f). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(g)the Plant Protection Products (Fees and Charges) Regulations 2011 M4;

(h)the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations 2013 M5;

F4(i). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(j)the Genetically Modified Organisms (Contained Use) Regulations 2014 M6;

(k)the Control of Major Accident Hazards Regulations 2015 M7;

F5(l). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

F6(m). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

F7(n). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

F8(o). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

(p)the Health and Safety and Nuclear (Fees) Regulations 2016 M8.

(2) Schedule 2 contains amendments to the following retained direct EU legislation—

(a)Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH);

(b)Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and mixtures;

(c)Commission Regulation (EU) No 544/2011 of 10 June 2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for active substances;

(d)Commission Regulation (EU) No 545/2011 of 10 June 2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards the data requirements for plant protection products;

(e)Commission Regulation (EU) No 547/2011 of 8 June 2011 implementing Regulation (EC) No 1107/2009 of the European Parliament and of the Council as regards labelling requirements for plant protection products;

(f)Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products;

(g)Regulation (EU) No 649/2012 of the European Parliament and of the Council of 4 July 2012 concerning the export and import of hazardous chemicals;

(h)Commission Regulation (EU) No 283/2013 of 1 March 2013 setting out the data requirements for active substances, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market;

(i)Commission Regulation (EU) No 284/2013 of 1 March 2013 setting out the data requirements for plant protection products, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market;

(j)Commission Implementing Regulation (EU) No 354/2013 of 18 April 2013 on changes of biocidal products authorised in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council;

(k)Commission Implementing Regulation (EU) No 414/2013 of 6 May 2013 specifying a procedure for the authorisation of same biocidal products in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council;

(l)Commission Implementing Regulation (EU) No 88/2014 of 31 January 2014 specifying a procedure for the amendment of Annex I to Regulation (EU) No 528/2012 of the European Parliament and of the Council concerning the making available on the market and use of biocidal products;

(m)Commission Delegated Regulation (EU) No 1062/2014 of 4 August 2014 on the work programme for the systematic examination of all existing active substances contained in biocidal products referred to in Regulation (EU) No 528/2012 of the European Parliament and of the Council.

(3) Schedule 3 contains amendments to Part 2 of Annex II to the EEA agreement.

Textual Amendments

Commencement Information

I1Reg. 2 in force at 31.12.2020 on IP completion day (in accordance with 2020 c. 1, Sch. 5 para. 1(1)), see reg. 1(2)

Marginal Citations