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Commission notice – Application of the Union’s pharmaceutical acquis in markets historically dependent on medicines supply from or through Great Britain after the end of the transition period 2020/C 447/05
C/2020/9264
- CELEX number:
- 52020XC1223(03)
- Form:
- Notice
- Legal basis:
- Author:
- European Commission, Directorate-General for Health and Food Safety
- Date of document:
- 23/12/2020; Date of publication
- Number of pages:
- 6
European Parliament resolution of 14 February 2017 on promoting gender equality in mental health and clinical research (2016/2096(INI))
- CELEX number:
- 52017IP0028
- Form:
- Own-initiative resolution
- Legal basis:
- Author:
- European Parliament, Committee on Development, Committee on Industry, Research and Energy, Committee on Women’s Rights and Gender Equality
- Date of document:
- 14/02/2017; Date of vote
- Number of pages:
- 14
Communication from the Commission — Detailed guidance on the collection, verification and presentation of adverse event/reaction reports arising from clinical trials on medicinal products for human use ( ‘CT-3’ )
- CELEX number:
- 52011XC0611(01)
- Form:
- Communication
- Legal basis:
- 32001L0020 - A09P8
- Author:
- European Commission
- Date of document:
- 11/06/2011; Date of publication
- Number of pages:
- 13
Communication from the Commission — Detailed guidance on the request to the competent authorities for authorisation of a clinical trial on a medicinal product for human use, the notification of substantial amendments and the declaration of the end of the trial (CT-1)
- CELEX number:
- 52010XC0330(01)
- Form:
- Communication
- Legal basis:
- 32001L0020 - A09P8
- Author:
- European Commission
- Date of document:
- 30/03/2010; Date of publication
- Number of pages:
- 19
Communication from the Commission regarding the guideline on the data fields contained in the clinical trials database provided for in Article 11 of Directive 2001/20/EC to be included in the database on medicinal products provided for in Article 57 of Regulation (EC) No 726/2004
- CELEX number:
- 52008XC0703(02)
- Form:
- Communication
- Legal basis:
- 32001L0020 - A57
- 32004R0726 - A11
- Author:
- European Commission
- Date of document:
- 03/07/2008; Date of publication
- Number of pages:
- 2
Commission Directive 2005/28/EC of 8 April 2005 laying down principles and detailed guidelines for good clinical practice as regards investigational medicinal products for human use, as well as the requirements for authorisation of the manufacturing or importation of such products (Text with EEA relevance)
In force
- CELEX number:
- 32005L0028
- Form:
- Directive
- Legal basis:
- 32001L0020 - A01P3 32001L0020 - A13P1 32001L0020 - A15P5
- Author:
- European Commission
- Date of document:
- 08/04/2005
- Number of pages:
- 7
Domain: All, Legal basis – CELEX number: 32001L0020, Search language: English