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Corrigendum to Commission Delegated Regulation (EU) No 1252/2014 of 28 May 2014 supplementing Directive 2001/83/EC of the European Parliament and of the Council with regard to principles and guidelines of good manufacturing practice for active substances for medicinal products for human use
Edition 2015-10-06

Regulation

EUV 2016/161

Commission Delegated Regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use
Edition 2015-10-02

Guidelines of 19 March 2015 on principles of Good Distribution Practice of active substances for medicinal products for human use
Edition 2015-03-19

Administrative provision

2009/53/EG

Directive 2009/53/EC of the European Parliament and of the Council of 18 June 2009 amending Directive 2001/82/EC and Directive 2001/83/EC, as regards variations to the terms of marketing authorisations for medicinal products
Edition 2009-06-18

Administrative provision

2003/63/EGBer

Corrigendum to Commission Directive 2003/63/EC of 25 June 2003 amending Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use
Edition 2003-11-20

Administrative provision

2003/63/EG

Commission Directive 2003/63/EC of 25 June 2003 amending Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use
Edition 2003-06-25

Administrative provision

Europarat/WHOEmpfBlutBek

Bekanntmachung der Empfehlungen des Europarates und der Weltgesundheitsorganisation zu Blut und Blutzubereitungen - Leitfaden für die Zubereitung, Anwendung und Qualitätssicherung von Blutbestandteilen
Edition 1995-12-01

Regulation

EUV 2019/5

Regulation (eu) 2019/5 of the European Parliament and of the Council of 11 December 2018 amending Regulation (EC) No 726/2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency, Regulation (EC) No 1901/2006 on medicinal products for paediatric use and Directive 2001/83/EC on the Community code relating to medicinal products for human use
Edition 2018-12-11

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