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European Union legislation
Medicinal products for human or veterinary uses
(Last revised:
August 19, 2010
)
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)
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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)
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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)
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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
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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)
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File (text of the
Official Journal - from the EUR-Lex
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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)
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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)
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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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