# The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019, Regulation 2: Amendments to retained EU law


(1) Schedule 1 contains amendments to the following subordinate legislation—
(a) the Health and Safety (Enforcing Authority) Regulations 1998;
(b) the Health and Safety (Enforcing Authority) Regulations (Northern Ireland) 1999;
(c) the Control of Substances Hazardous to Health Regulations 2002;
(d) the Dangerous Substances and Explosive Atmospheres Regulations 2002;
(e) the Control of Substances Hazardous to Health Regulations (Northern Ireland) 2003;
(f) the Dangerous Substances and Explosive Atmospheres Regulations (Northern Ireland) 2003;
(g) the Plant Protection Products (Fees and Charges) Regulations 2011;
(h) the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations 2013;
(i) the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations (Northern Ireland) 2013;
(j) the Genetically Modified Organisms (Contained Use) Regulations 2014;
(k) the Control of Major Accident Hazards Regulations 2015;
(l) the Explosives (Appointment of Authorities and Enforcement) Regulations (Northern Ireland) 2015;
(m) the Biocidal Products (Fees and Charges) Regulations (Northern Ireland) 2015;
(n) the Control of Major Accident Hazards Regulations (Northern Ireland) 2015;
(o) the Genetically Modified Organisms (Contained Use) Regulations (Northern Ireland) 2015;
(p) the Health and Safety and Nuclear (Fees) Regulations 2016.
(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.

---
Source: https://www.legislation.gov.uk/ukdsi/2019/9780111181539/regulation/2 (the official version)
Page: https://openlegislation.uk/draft-chemicals-health-and-safety-and-genetically-modified-organisms-contained-use-amendment-etc-eu-exit-regulations-2019/regulation-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.