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European Union legislation
Medicinal products for human or veterinary uses

(Last revised: August 19, 2010 )

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* COMMISSION DIRECTIVE 2009/120/EC of 14 September 2009 amending Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use as regards advanced therapy medicinal products.
(OJL 242, 15.09.2009, p.3)
PDF File (text of the Official Journal - from the EUR-Lex Web Site)

* 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.
(OJL 324, 10.12.2007, p.121)
PDF File (text of the Official Journal - from the EUR-Lex Web Site)

* 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.
(OJ L 136, 30.4.2004, p.1)
PDF File (text of the Official Journal - from the EUR-Lex Web Site)

* DIRECTIVE 2004/28/EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001/82/EC on the Community code relating to veterinary medicinal products.
(OJ L 136, 30.4.2004, p.58)
PDF File (text of the Official Journal - from the EUR-Lex Web Site)

* DIRECTIVE 2004/27/EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use.
(OJ L 136, 30.4.2004, p.34)
PDF File (text of the Official Journal - from the EUR-Lex Web Site)

* 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.
(OJ L 159, 27.6.2003, p.46)
PDF File (text of the Official Journal - from the EUR-Lex Web Site)

* COUNCIL REGULATION (EC) No 1647/2003 of 18 June 2003 amending Regulation (EEC) No 2309/93 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Agency for the evaluation of Medicinal Products.
(OJ L 245, 29.9.2003, p.19)
PDF File (text of the Official Journal - from the EUR-Lex Web Site)

* 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.
(OJ L 311, 28.11.2001, p.67)
PDF File (text of the Official Journal - from the EUR-Lex Web Site)

* DIRECTIVE 2001/82/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to veterinary medicinal products.
(OJ L 311, 28.11.2001, p.1)
PDF File (text of the Official Journal - from the EUR-Lex Web Site)

* DIRECTIVE 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use.
(OJ L 121, 1.05.2001, p.34)
PDF File (text of the Official Journal - from the EUR-Lex Web Site)

* COUNCIL REGULATION (EEC) No 2309/93 of 22 July 1993 laying down Community procedures for the authorization and supervision of medicinal products for human and veterinary use and establishing a European Agency for the Evaluation of Medicinal Products.
(OJ L 214, 24.08.1993, p.1)
Note: This Regulation has been repealed and replaced by Regulation (EC) No 726/2004 of 31 March 2004.

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