Amendments to retained EU law2

1

Schedule 1 contains amendments to the following subordinate legislation—

a

the Health and Safety (Enforcing Authority) Regulations 19982;

b

the Health and Safety (Enforcing Authority) Regulations (Northern Ireland) 19993;

c

the Control of Substances Hazardous to Health Regulations 20024;

d

the Dangerous Substances and Explosive Atmospheres Regulations 20025;

e

the Control of Substances Hazardous to Health Regulations (Northern Ireland) 20036;

f

the Dangerous Substances and Explosive Atmospheres Regulations (Northern Ireland) 20037;

g

the Plant Protection Products (Fees and Charges) Regulations 20118;

h

the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations 20139;

i

the Biocidal Products and Chemicals (Appointment of Authorities and Enforcement) Regulations (Northern Ireland) 201310;

j

the Genetically Modified Organisms (Contained Use) Regulations 201411;

k

the Control of Major Accident Hazards Regulations 201512;

l

the Explosives (Appointment of Authorities and Enforcement) Regulations (Northern Ireland) 201513;

m

the Biocidal Products (Fees and Charges) Regulations (Northern Ireland) 201514;

n

the Control of Major Accident Hazards Regulations (Northern Ireland) 201515;

o

the Genetically Modified Organisms (Contained Use) Regulations (Northern Ireland) 201516;

p

the Health and Safety and Nuclear (Fees) Regulations 201617.

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.