European Communities (Clinical Trials on Medicinal Products For Human Use) Regulations, 2004
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European Communities (Clinical Trials on Medicinal Products For Human Use) Regulations, 2004
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- Medicinal Products (Amendment) Regulations, 1999
- 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
- 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
- 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
- Medical Preparations (Licensing of Manufacture) Regulations, 1993
