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Regulation (EU) 2024/568 of the European Parliament and of the Council of 7 February 2024 on fees and charges payable to the European Medicines Agency, amending Regulations (EU) 2017/745 and (EU) 2022/123 of the European Parliament and of the Council and repealing Regulation (EU) No 658/2014 of the European Parliament and of the Council and Council Regulation (EC) No 297/95
PE/59/2023/REV/1
In force
- CELEX number:
- 32024R0568
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 07/02/2024; Date of signature
Regulation (EU) 2023/1182 of the European Parliament and of the Council of 14 June 2023 on specific rules relating to medicinal products for human use intended to be placed on the market in Northern Ireland and amending Directive 2001/83/EC (Text with EEA relevance)
PE/20/2023/REV/2
In force
- CELEX number:
- 32023R1182
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 14/06/2023; Date of signature
- Number of pages:
- 7
Regulation (EU) 2022/123 of the European Parliament and of the Council of 25 January 2022 on a reinforced role for the European Medicines Agency in crisis preparedness and management for medicinal products and medical devices (Text with EEA relevance)
PE/76/2021/REV/1
In force
- CELEX number:
- 32022R0123
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 25/01/2022; Date of signature
- Number of pages:
- 37
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) 2016/793 of the European Parliament and of the Council of 11 May 2016 to avoid trade diversion into the European Union of certain key medicines (codification)
In force
- CELEX number:
- 32016R0793
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 11/05/2016; Date of signature
- Number of pages:
- 16
Regulation (EU) No 658/2014 of the European Parliament and of the Council of 15 May 2014 on fees payable to the European Medicines Agency for the conduct of pharmacovigilance activities in respect of medicinal products for human use Text with EEA relevance
In force
- CELEX number:
- 32014R0658
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 15/05/2014
- Number of pages:
- 16
Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC Text with EEA relevance
In force
- CELEX number:
- 32014R0536
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 16/04/2014
- Number of pages:
- 76
Directive 2011/62/EU of the European Parliament and of the Council of 8 June 2011 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use, as regards the prevention of the entry into the legal supply chain of falsified medicinal products Text with EEA relevance
In force
- CELEX number:
- 32011L0062
- Form:
- Directive
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 08/06/2011
- Number of pages:
- 14
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
Domain: All, EUROVOC descriptor: medicinal product, Search language: English