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Regulation

EUV 2020/1593

Commission Regulation (EU) 2020/1593 of 29 October 2020 amending Annex X to Regulation (EC) No 999/2001 of the European Parliament and of the Council as regards further examination of positive cases of transmissible spongiform encephalopathies in ovine and caprine animals
Edition 2020-10-29

Regulation

EUV 2021/756

Commission Delegated Regulation (EU) 2021/756 of 24 March 2021 amending Regulation (EC) No 1234/2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products
Edition 2021-03-24

Corrigendum to 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
Edition 2023-01-26

Regulation

EUV 1062/2014

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
Edition 2014-08-04

Administrative provision

EU 2015/254

Directive (EU) 2015/254 of the European Parliament and of the Council of 11 February 2015 repealing Council Directive 93/5/EEC on assistance to the Commission and cooperation by the Member States in the scientific examination of questions relating to food
Edition 2015-02-11

Corrigendum to 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
Edition 2015-07-28

Regulation

EUV 712/2012

Commission Regulation (EU) No 712/2012 of 3 August 2012 amending Regulation (EC) No 1234/2008 concerning the examination of variations to the terms of marketing authorisations for medicinal products for human use and veterinary medicinal products
Edition 2012-08-03

Regulation

EUV 736/2013

Commission Delegated Regulation (EU) No 736/2013 of 17 May 2013 amending Regulation (EU) No 528/2012 of the European Parliament and of the Council as regards the duration of the work programme for examination of existing biocidal active substances
Edition 2013-05-17

Ordinance for the amendment to the ordinance on the competences according to the Pharmacies Act, the Pharmaceutical Products Act, the Narcotics Act, the Federal Regulations on Pharmacies, the Licensing Regulations for Pharmacies, the Act on the profession of pharmaceutic-technical assistants and the training and examination regulations for pharmaceutic-technical assistants
Edition 1982-09-08

Administrative provision

96/341/EGEntsch

Commission Decision of 20 May 1996 recognizing in principle the completeness of the dossier submitted for detailed examination in view of the possible inclusion of flurtamone in Annex I of Council Directive 91/414/EEC concerning the placing of plant protection products on the market (Text with EEA relevance)
Edition 1996-05-20

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