The Medicines for Human Use (Clinical Trials) and Blood Safety and Quality (Amendment) Regulations 2008

Statutory instruments 2008 941

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TSO (The Stationery Office)

Enabling power: European Communities Act 1972, s. 2 (2) Issued: 07.04.2008. Made: 31.03.2008. Laid: 07.04.2008. Coming into force: 01.05.2008. Effect: S.I. 2004/1031; 2005/50 amended. Territorial extent & classification: E/W/S/NI. General EC note: These Regulations amend the Medicines for Human Use (Clinical Trials) Regulations 2004 (the Clinical Trials Regulations) which implement Directive 2001/20/EC 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. This includes updating the definition of the Clinical Trials Directive and Directive 2001/83/EC respectively to take account of the subsequent amendment of those Directives by Community Regulations

Extent	8p.	ISBN	9780110813257
Size	N/A	Price	£8.14
Format	Paperback	Published	07 Apr 2008
Availability	Black and white copy, 1-3 days	Delivery	Delivery options and charges