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Commission Communication on the results of the risk evaluation and the risk reduction strategies for the substances: Dibutylphthalate; 3,4-Dichloroaniline; Di-'isodecyl' phthalate; 1,2-Benzenedicarboxylic acid, di-C9-11-branched alkyl esters, C10-rich; Di-'isononyl' phthalate; 1,2-Benzenedicarboxylic acid, di-C8-10-branched alkyl esters, C9-rich; Ethylenediaminetetraacetate; Methyl acetate; Monochloroacetic acid; n-Pentane; Tetrasodium ethylenediaminetetraacetate
Edition 2006-04-13

Regulation

EUV 2020/2034

Commission Delegated Regulation (EU) 2020/2034 of 6 October 2020 supplementing Regulation (EU) No 376/2014 of the European Parliament and of the Council as regards the common European risk classification scheme
Edition 2020-10-06

Administrative provision

EU 2019/782

Commission Directive (EU) 2019/782 of 15 May 2019 amending Directive 2009/128/EC of the European Parliament and of the Council as regards the establishment of harmonised risk indicators
Edition 2019-05-15

Administrative provision

EU 2018/350

Commission Directive (EU) 2018/350 of 8 March 2018 amending Directive 2001/18/EC of the European Parliament and of the Council as regards the environmental risk assessment of genetically modified organisms
Edition 2018-03-08

Administrative provision

EUB 2018/1790

Commission Implementing Decision (EU) 2018/1790 of 16 November 2018 repealing Decision 2002/623/EC establishing guidance notes on the environmental risk assessment of genetically modified organisms
Edition 2018-11-16

Administrative provision

EUB 2022/729

Commission Implementing Decision (EU) 2022/729 of 11 May 2022 amending Implementing Decision (EU) 2021/1195 as regards harmonised standards for quality management systems and for application of risk management to medical devices
Edition 2022-05-11

Administrative provision

EUB 2022/757

Commission Implementing Decision (EU) 2022/757 of 11 May 2022 amending Implementing Decision (EU) 2021/1182 as regards harmonised standards for quality management systems, sterilisation and application of risk management to medical devices
Edition 2022-05-11

Regulation

EUV 2022/517

Commission Delegated Regulation (EU) 2022/517 of 18 November 2021 amending Regulation (EU) 2017/1938 of the European Parliament and of the Council as regards the composition of the risk groups
Edition 2021-11-18

Regulation

EUV 2021/842

Commission Implementing Regulation (EU) 2021/842 of 26 May 2021 amending Implementing Regulation (EU) No 307/2012 as regards transparency and confidentiality requirements for the EU risk assessment of substances under scrutiny
Edition 2021-05-26

Corrigendum to Commission Implementing Regulation (EU) 2015/1136 of 13 July 2015 amending Implementing Regulation (EU) No 402/2013 on the common safety method for risk evaluation and assessment
Edition 2016-03-16

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