The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019

Amendments to retained EU law

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

(a) the Health and Safety (Enforcing Authority) Regulations 1998(1);

(b) the Health and Safety (Enforcing Authority) Regulations (Northern Ireland) 1999(2);

(c) the Control of Substances Hazardous to Health Regulations 2002(3);

(d) the Dangerous Substances and Explosive Atmospheres Regulations 2002(4);

(e) the Control of Substances Hazardous to Health Regulations (Northern Ireland) 2003(5);

(f) the Dangerous Substances and Explosive Atmospheres Regulations (Northern Ireland) 2003(6);

(g) the Plant Protection Products (Fees and Charges) Regulations 2011(7);

(h) the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations 2013(8);

(i) the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations (Northern Ireland) 2013(9);

(j) the Genetically Modified Organisms (Contained Use) Regulations 2014(10);

(k) the Control of Major Accident Hazards Regulations 2015(11);

(l) the Explosives (Appointment of Authorities and Enforcement) Regulations (Northern Ireland) 2015(12);

(m) the Biocidal Products (Fees and Charges) Regulations (Northern Ireland) 2015(13);

(n) the Control of Major Accident Hazards Regulations (Northern Ireland) 2015(14);

(o) the Genetically Modified Organisms (Contained Use) Regulations (Northern Ireland) 2015(15);

(p) the Health and Safety and Nuclear (Fees) Regulations 2016(16).

(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.

(1)

S.I. 1998/494, amended by S.I. 2015/21.

(2)

S.R. 1999 No. 90, amended by S.R. 2015 No. 265.

(3)

S.I. 2002/2677, amended by S.I. 2015/21.

(4)

S.I. 2002/2776, amended by S.I. 2015/21.

(5)

S.R. 2003 No. 34, amended by S.R. 2015 No. 265.

(6)

S.R. 2003 No. 152, amended by S.R. 2015 No. 265.

(7)

S.I. 2011/2132, amended by S.I. 2016/254.

(8)

S.I. 2013/1506.

(9)

S.R. 2013 No.206.

(10)

S.I. 2014/1663, amended by S.I. 2015/1637.

(11)

S.I. 2015/483.

(12)

S.R. 2015 No. 236.

(13)

S.R. 2015 No. 254.

(14)

S.R. 2015 No. 325.

(15)

S.R. 2015 No. 339.

(16)

S.I. 2016/253.