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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

CELEX number:
32017R0746
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

CELEX number:
31998L0079
Author:
European Parliament, Council of the European Union
Date of document:
27/10/1998

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
Author:
European Parliament, Council of the European Union
Date of document:
16/04/2014

Regulation (EU) No 282/2014 of the European Parliament and of the Council of 11 March 2014 on the establishment of a third Programme for the Union's action in the field of health (2014-2020) and repealing Decision No 1350/2007/EC Text with EEA relevance

In force

CELEX number:
32014R0282
Author:
European Parliament, Council of the European Union
Date of document:
11/03/2014

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

CELEX number:
32004L0023
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

CELEX number:
32002L0098
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

CELEX number:
32011L0024
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

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

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
Author:
European Parliament, Council of the European Union
Date of document:
06/11/2001

Directive 2010/45/EU of the European Parliament and of the Council of 7 July 2010 on standards of quality and safety of human organs intended for transplantation

In force

CELEX number:
32010L0053
Author:
European Parliament, Council of the European Union
Date of document:
07/07/2010
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