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Domain: All, EUROVOC descriptor: medicinal product, Search language: English
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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

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

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

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

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

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

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

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

Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004 (Text with EEA relevance)

In force

CELEX number:
32007R1394
Form:
Regulation
Author:
European Parliament, Council of the European Union
Date of document:
13/11/2007

Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance)

In force

CELEX number:
32004R0726
Form:
Regulation
Author:
European Parliament, Council of the European Union
Date of document:
31/03/2004
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