Regulation 2 Amendments to retained EU lawI1
United Kingdom
Schedule 1 contains amendments to the following subordinate legislation—
the Health and Safety (Enforcing Authority) Regulations 1998 M1;
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the Control of Substances Hazardous to Health Regulations 2002 M2;
the Dangerous Substances and Explosive Atmospheres Regulations 2002 M3;
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the Plant Protection Products (Fees and Charges) Regulations 2011 M4;
the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations 2013 M5;
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the Genetically Modified Organisms (Contained Use) Regulations 2014 M6;
the Control of Major Accident Hazards Regulations 2015 M7;
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the Health and Safety and Nuclear (Fees) Regulations 2016 M8.
Schedule 2 contains amendments to the following retained direct EU legislation—
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);
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;
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;
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;
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;
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;
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;
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;
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;
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;
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;
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;
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.
Schedule 3 contains amendments to Part 2 of Annex II to the EEA agreement.
Annotations
Textual amendments
- F1
Reg. 2(1)(b) omitted (31.12.2020 immediately before IP completion day) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1567), regs. 1(2), 4(a)
- F2
Reg. 2(1)(e) omitted (31.12.2020 immediately before IP completion day) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1567), regs. 1(2), 4(b)
- F3
Reg. 2(1)(f) omitted (31.12.2020 immediately before IP completion day) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1567), regs. 1(2), 4(c)
- F4
Reg. 2(1)(i) omitted (31.12.2020 immediately before IP completion day) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1567), regs. 1(2), 4(d)
- F5
Reg. 2(1)(l) omitted (31.12.2020 immediately before IP completion day) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1567), regs. 1(2), 4(e)
- F6
Reg. 2(1)(m) omitted (31.12.2020 immediately before IP completion day) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1567), regs. 1(2), 4(f)
- F7
Reg. 2(1)(n) omitted (31.12.2020 immediately before IP completion day) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1567), regs. 1(2), 4(g)
- F8
Reg. 2(1)(o) omitted (31.12.2020 immediately before IP completion day) by virtue of The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1567), regs. 1(2), 4(h)
Marginal citations
- M1
S.I. 1998/494, amended by S.I. 2015/21.
- M2
S.I. 2002/2677, amended by S.I. 2015/21.
- M3
S.I. 2002/2776, amended by S.I. 2015/21.
- M4
S.I. 2011/2132, amended by S.I. 2016/254.
- M5
- M6
S.I. 2014/1663, amended by S.I. 2015/1637.
- M7
- M8
Commencement
- I1
Reg. 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)