Commission Implementing Decision (EU) 2021/2174 of 3 December 2021 on unresolved objections regarding the terms and conditions of the authorisation of the biocidal product Konservan P40 in accordance with Article 36(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2021) 8686) (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）第36（1）条（根据C（2021）8686号文件通知） 委员会于2021 12月3日就关于杀生物产品Konservan P40的授权条款和条件的未解决异议作出的2021第2174号实施决定（EU）（与EEA相关的文本）

2021-12-03

Commission Implementing Decision (EU) 2021/2165 of 3 December 2021 concerning the extension of the action taken by the Ministry of Health of the Czech Republic permitting the making available on the market and use of the biocidal product Biobor JF in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2021) 8684) (Only the Czech text is authentic)
根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条（根据C（2021）8684号文件通知） 委员会于2021 12月3日通过的关于延长捷克共和国卫生部采取的允许在市场上提供和使用杀生物产品Biobor JF的行动的委员会执行决定（EU）2021/2165（只有捷克语文本是真实的）

2021-12-03

Commission Implementing Decision (EU) 2016/1174 of 15 July 2016 on the terms and conditions of the authorisation of a biocidal product containing difenacoum referred by Spain in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2016) 4380) (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）第36条（根据C（2016）4380号文件通知） 委员会于2016年7月15日就西班牙提及的含有杀生物剂的杀生物产品的授权条款和条件作出的第2016/1174号实施决定（EU）（与EEA相关的文本）

2016-07-15

Commission Implementing Decision (EU) 2015/1751 of 29 September 2015 on the terms and conditions of the authorisation of a biocidal product containing bromadiolone referred by the United Kingdom in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2015) 6516) (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）第36条（根据C（2015）6516号文件通知） 委员会于2015年9月29日就联合王国提及的含有溴敌隆的杀生物产品的授权条款和条件作出了第2015/1751号实施决定（EU）（与EEA相关的文本）

2015-09-29

Commission Implementing Decision (EU) 2016/1175 of 15 July 2016 on the terms and conditions of the authorisation of a biocidal product containing spinosad referred by the United Kingdom in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2016) 4385) (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）第36条（根据C（2016）4385号文件通知） 委员会于2016年7月15日通过了关于英国提及的含有多杀菌素的杀生物产品的授权条款和条件的第2016/1175号实施决定（EU）（与EEA相关的文本）

2016-07-15

Commission Implementing Decision (EU) 2022/323 of 22 February 2022 on the unresolved objections regarding the conditions for granting an authorisation for the biocidal product Sojet in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2022) 973) (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）（根据C（2022）973号文件通知）的规定 委员会于2022年2月22日就关于批准杀生物产品Sojet的条件的未解决异议作出的第2022/323号实施决定（EU）（与EEA相关的文本）

2022-02-22

Commission Implementing Decision (EU) 2017/810 of 10 May 2017 on a derogation from mutual recognition of the authorisation of a biocidal product containing boric acid by France in accordance with Article 37 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2017) 2935)
根据欧洲议会和理事会第528/2012号法规（EU）第37条（根据C（2017）2935号文件通知） 委员会2017年5月10日第2017/810号执行决定（EU）减损法国对含有硼酸的杀生物产品的授权的相互承认

2017-05-10

Commission Implementing Decision (EU) 2021/2185 of 6 December 2021 concerning the extension of the action taken by the Health and Safety Executive of the United Kingdom permitting the making available on the market and use of the biocidal product Micronclean Hand Sanitiser in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2021) 8736) (Only the English text is a
根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条的规定 委员会于2021 12月6日通过了第2021/2185号实施决定（EU） 该决定涉及延长英国健康与安全执行局采取的行动 允许在市场上提供和使用杀生物产品Micronclean洗手液（根据文件C（2021）8736通知）（只有英文文本是

2021-12-06

Commission Delegated Decision (EU) 2021/2183 of 25 August 2021 amending Annex V to Directive 2005/36/EC of the European Parliament and of the Council as regards the evidence of formal qualifications and titles of training courses (notified under document C(2021) 6111) (Text with EEA relevance)
委员会2021 8月25日第2021/2183号授权决定（EU）2021修订了欧洲议会和理事会指令2005/36/EC关于培训课程正式资格和名称的证据的附件五（根据文件C（2021）6111通知）（与欧洲经济区相关的文本）

2021-08-25

Commission Implementing Decision (EU) 2018/1297 of 25 September 2018 on a derogation from mutual recognition of the authorisation of biocidal products containing creosote by France in accordance with Article 37 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2018) 5412)
根据欧洲议会和理事会第528/2012号法规（EU）第37条（根据C（2018）5412号文件通知） 委员会于2018年9月25日通过了第2018/1297号执行决定（EU） 该决定涉及法国对含有杂酚油的杀生物产品的授权相互承认的减损

2018-09-25

Commission Implementing Decision (EU) 2016/2318 of 16 December 2016 on a derogation from mutual recognition of the authorisations of biocidal products containing brodifacoum by Spain in accordance with Article 37 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2016) 8414)
根据欧洲议会和理事会第528/2012号法规（欧盟）第37条（根据C（2016）8414号文件通知） 委员会2016年12月16日第2016/2318号执行决定（欧盟）关于减损西班牙对含有溴代法康的杀生物产品的授权的相互承认

2016-12-16

Commission Implementing Decision (EU) 2021/2184 of 6 December 2021 concerning the extension of the actions taken by the Health and Safety Executive of the United Kingdom permitting the making available on the market and use of five biocidal products for hand disinfection in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2021) 8729) (Only the English text is aut
根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条的规定 委员会于2021 12月6日通过了第2021/2184号实施决定（EU） 该决定涉及延长英国健康与安全执行局采取的行动 允许在市场上提供和使用五种用于手部消毒的生物杀菌产品（根据文件C（2021）8729通知）（只有英文文本为aut

2021-12-06

Commission Implementing Decision (EU) 2017/721 of 20 April 2017 concerning the extension of the action taken by Sweden on the making available on the market and use of the biocidal product VectoBac 12AS in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2017) 2435)
2017年4月20日委员会执行决定（EU）2017/721 涉及根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条（根据C（2017）2435号文件通知）延长瑞典在市场上提供和使用杀生物产品VectoBac 12的行动

2017-04-20

Commission Implementing Decision (EU) 2017/722 of 20 April 2017 concerning the extension of the action taken by the Netherlands on the making available on the market and use of the biocidal product VectoMaxFG in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2017) 2436)
2017年4月20日委员会执行决定（EU）2017/722 关于延长荷兰根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条（根据C（2017）2436号文件通知）在市场上提供和使用杀生物产品VectoMaxFG所采取的行动

2017-04-20

Commission Implementing Decision (EU) 2016/714 of 11 May 2016 concerning the extension of the action taken by the Netherlands on the making available on the market and use of the biocidal products VectoBacWG and Aqua-K-Othrine in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2016) 2682)
根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条（根据C（2016）2682号文件通知） 委员会2016年5月11日关于延长荷兰在市场上提供和使用生物杀灭产品VectoBacWG和Aqua-K-Othrine的行动的第2016/714号实施决定（EU）

2016-05-11

Commission Implementing Decision (EU) 2018/1477 of 2 October 2018 on the terms and conditions of the authorisations of biocidal products containing ethyl butylacetylaminopropionate referred by Belgium in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2018) 6291) (Text with EEA relevance.)
委员会2018年10月2日第2018/1477号执行决定（欧盟） 关于比利时根据欧洲议会和理事会第528/2012号法规（欧盟）第36条（根据C（2018）6291号文件通知）提交的含有丁乙酰氨基丙酸乙酯的杀生物产品的授权条款和条件（与欧洲经济区相关的文本）

2018-10-02

Commission Implementing Decision (EU) 2018/232 of 15 February 2018 concerning the extension of the action taken by Belgium on the making available on the market and use of the biocidal products VectoMax G and Aqua-K-Othrine in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2018) 759)
根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条（根据C（2018）759号文件通知） 委员会2018年2月15日第2018/232号执行决定（EU）关于延长比利时在市场上提供和使用杀生物产品VectoMax G和Aqua-K-Othrine方面采取的行动

2018-02-15

Commission Implementing Decision (EU) 2022/2054 of 21 October 2022 on the unresolved objections regarding the conditions for granting an authorisation for the biocidal product Preventol A 12 TK 50 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2022) 7408) (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）（根据文件C（2022）7408通知） 委员会执行2022年10月21日第2022/2054号决定 该决定针对授予生物杀灭剂产品Preventol A 12 TK 50授权条件的未解决异议（与欧洲经济区相关的文本）

2022-10-21

Commission Implementing Decision (EU) 2018/1305 of 26 September 2018 on the terms and conditions of the authorisation of a biocidal product family containing deltamethrin referred by Sweden in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document number C(2018) 5503) (Text with EEA relevance.)
委员会2018年9月26日第2018/1305号执行决定（欧盟） 涉及瑞典根据欧洲议会和理事会第528/2012号法规（欧盟）第36条提交的含有溴氰菊酯的杀生物产品系列的授权条款和条件（根据C（2018）5503号文件通知）（与欧洲经济区相关的文本）

2018-09-26

Commission Implementing Decision (EU) 2018/696 of 4 May 2018 concerning the extension of the action taken by the French Ministry of Environment, Energy and Sea, in charge of international negotiations on climate permitting the making available on the market and use of the biocidal product Phéro-Ball Pin in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2018) 26
委员会2018年5月4日关于延长法国环境、能源和海洋部所采取行动的第2018/696号执行决定（欧盟） 负责根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条（根据C（2018）26号文件通知） 就允许市场上提供和使用杀生物产品Phero球销的气候问题进行国际谈判

2018-05-04