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Search for: medical devices, Search language: English
Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (Text with EEA relevance. )
In force
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- CELEX number:
- 32017R0746
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 05/04/2017; Date of signature
Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices
In force
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- CELEX number:
- 31998L0079
- Form:
- Directive
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 27/10/1998
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
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- CELEX number:
- 32022R0123
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 25/01/2022; Date of signature
Regulation (EU) 2021/2282 of the European Parliament and of the Council of 15 December 2021 on health technology assessment and amending Directive 2011/24/EU (Text with EEA relevance)
PE/80/2021/INIT
In force
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- CELEX number:
- 32021R2282
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 15/12/2021; Date of signature
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
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- CELEX number:
- 32014R0536
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 16/04/2014
Directive 2004/23/EC of the European Parliament and of the Council of 31 March 2004 on setting standards of quality and safety for the donation, procurement, testing, processing, preservation, storage and distribution of human tissues and cells
In force
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- CELEX number:
- 32004L0023
- Form:
- Directive
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 31/03/2004
Directive 2002/98/EC of the European Parliament and of the Council of 27 January 2003 setting standards of quality and safety for the collection, testing, processing, storage and distribution of human blood and blood components and amending Directive 2001/83/EC
In force
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- CELEX number:
- 32002L0098
- Form:
- Directive
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 27/01/2003
Directive 2011/24/EU of the European Parliament and of the Council of 9 March 2011 on the application of patients’ rights in cross-border healthcare
In force
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- CELEX number:
- 32011L0024
- Form:
- Directive
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 09/03/2011
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
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- CELEX number:
- 32007R1394
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 13/11/2007
Regulation (EU) 2022/2371 of the European Parliament and of the Council of 23 November 2022 on serious cross-border threats to health and repealing Decision No 1082/2013/EU (Text with EEA relevance)
PE/40/2022/REV/1
In force
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- CELEX number:
- 32022R2371
- Form:
- Regulation
- Author:
- European Parliament, Council of the European Union
- Date of document:
- 23/11/2022; Date of signature