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Regulation (EU) 2022/839 of the European Parliament and of the Council of 30 May 2022 laying down transitional rules for the packaging and labelling of veterinary medicinal products authorised or registered in accordance with Directive 2001/82/EC or Regulation (EC) No 726/2004 (Text with EEA relevance)
PE/19/2022/REV/1
In force
- CELEX number:
- 32022R0839
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 30/05/2022; Date of signature
- Number of pages:
- 2
Regulation (EU) 2020/1043 of the European Parliament and of the Council of 15 July 2020 on the conduct of clinical trials with and supply of medicinal products for human use containing or consisting of genetically modified organisms intended to treat or prevent coronavirus disease (COVID-19)
PE/28/2020/REV/1
In force
- CELEX number:
- 32020R1043
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 15/07/2020; Date of signature
- Number of pages:
- 5
Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance)
PE/45/2018/REV/1
In force
- CELEX number:
- 32019R0006
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 11/12/2018; Date of signature
- Number of pages:
- 125
Regulation (EC) No 469/2009 of the European Parliament and of the Council of 6 May 2009 concerning the supplementary protection certificate for medicinal products (Codified version) (Text with EEA relevance )
In force
- CELEX number:
- 32009R0469
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 06/05/2009
- Number of pages:
- 10
Directive 2009/35/EC of the European Parliament and of the Council of 23 April 2009 on the colouring matters which may be added to medicinal products (recast) (Text with EEA relevance)
In force
- CELEX number:
- 32009L0035
- Form:
- Directive
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 23/04/2009
- Number of pages:
- 4
Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use
In force
- CELEX number:
- 32001L0083
- Form:
- Directive
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 06/11/2001
- Number of pages:
- 62
Commission Delegated Regulation (EU) 2024/1159 of 7 February 2024 supplementing Regulation (EU) 2019/6 of the European Parliament and of the Council by laying down rules on appropriate measures to ensure the effective and safe use of veterinary medicinal products authorised and prescribed for oral administration via routes other than medicated feed and administered by the animal keeper to food-producing animals
C/2024/661
In force
- CELEX number:
- 32024R1159
- Form:
- Delegated regulation
- Author:
- European Commission, Directorate-General for Health and Food Safety
- Date of document:
- 07/02/2024; Date of adoption
Commission Implementing Regulation (EU) 2024/878 of 21 March 2024 adopting uniform rules on the size of small immediate packaging units of veterinary medicinal products as referred to in Article 12 of Regulation (EU) 2019/6 of the European Parliament and of the Council
C/2024/1601
In force
- CELEX number:
- 32024R0878
- Form:
- Implementing regulation
- Author:
- European Commission, Directorate-General for Health and Food Safety
- Date of document:
- 21/03/2024; Date of adoption
Commission Implementing Regulation (EU) 2024/875 of 21 March 2024 adopting a list of abbreviations and pictograms common throughout the Union to be used on the packaging of veterinary medicinal products for the purposes of Article 10(2) and Article 11(3) of Regulation (EU) 2019/6 of the European Parliament and of the Council
C/2024/1600
In force
- CELEX number:
- 32024R0875
- Form:
- Implementing regulation
- Author:
- European Commission, Directorate-General for Health and Food Safety
- Date of document:
- 21/03/2024; Date of adoption
Decision of the EEA Joint Committee No 179/2023 of 5 July 2023 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2024/800]
Date of entry into force unknown (pending notification) or not yet in force.
- CELEX number:
- 22024D0800
- Form:
- Decision adopted by bodies created by international agreements
- Author:
- EEA Joint Committee
- Date of document:
- 05/07/2023; Date of adoption
Domain: All, EUROVOC descriptor: pharmaceutical legislation, Search language: English