The Medicines for Human Use (Clinical Trials) Amendment Regulations 2006 Reprinted October 2006

Statutory instruments 1928 2006

Format:

Corporate Author:

Great Britain

Publisher:

TSO (The Stationery Office)

Enabling power: European Communities Act 1972, s. 2 (2). Issued: 20.07.2006. Made: 13.07.2006. Laid: 20.07.2006. Coming into force: 29.08.2006. Effect: S.I. 2004/1031 amended. Territorial extent and classification: E/W/S/NI. General. EC note: These Regulations amend the Medicines for Human Use (Clinical Trials) Regulations 2004 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 in human use. In particular, they implement Commission Directive 2005/28/EC laying down principles and detailed guidelines for good clinical practice as regards investigational medicinal products for human use, as well as the requirements for authorisation of the manufacturing or importation of such products (the GCP Directive) and make other miscellaneous amendments.

Extent	12p.	ISBN	9780110748610
Size	N/A	Price	£8.14
Format	Paperback	Published	20 Jul 2006
Availability	Black and white copy, 1-3 days	Delivery	Delivery options and charges