OpenLegislation

Regulation 2 Amendments to retained EU law

Original text. Later amendments are not shown.

(1)

Schedule 1 contains amendments to the following subordinate legislation—

(a)

the Health and Safety (Enforcing Authority) Regulations 1998f1;

(b)

the Health and Safety (Enforcing Authority) Regulations (Northern Ireland) 1999f2;

(c)

the Control of Substances Hazardous to Health Regulations 2002f3;

(d)

the Dangerous Substances and Explosive Atmospheres Regulations 2002f4;

(e)

the Control of Substances Hazardous to Health Regulations (Northern Ireland) 2003f5;

(f)

the Dangerous Substances and Explosive Atmospheres Regulations (Northern Ireland) 2003f6;

(g)

the Plant Protection Products (Fees and Charges) Regulations 2011f7;

(h)

the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations 2013f8;

(i)

the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations (Northern Ireland) 2013f9;

(j)

the Genetically Modified Organisms (Contained Use) Regulations 2014f10;

(k)

the Control of Major Accident Hazards Regulations 2015f11;

(l)

the Explosives (Appointment of Authorities and Enforcement) Regulations (Northern Ireland) 2015f12;

(m)

the Biocidal Products (Fees and Charges) Regulations (Northern Ireland) 2015f13;

(n)

the Control of Major Accident Hazards Regulations (Northern Ireland) 2015f14;

(o)

the Genetically Modified Organisms (Contained Use) Regulations (Northern Ireland) 2015f15;

(p)

the Health and Safety and Nuclear (Fees) Regulations 2016f16.

(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.

Annotations

Footnotes

f1

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

f2

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

f3

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

f4

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

f5

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

f6

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

f7

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

f8

S.I. 2013/1506.

f9

S.R. 2013 No.206.

f10

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

f11

S.I. 2015/483.

f12

S.R. 2015 No. 236.

f13

S.R. 2015 No. 254.

f14

S.R. 2015 No. 325.

f15

S.R. 2015 No. 339.

f16

S.I. 2016/253.