UK Parliament / Open data

European Parliament and Council Directive 2001/20/EC on the approximation of provisions laid down by law, regulation and administrative action relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use. Adopted 04.04.2001.

European material produced by EU institutions () published on Monday, 30 April 2001.

About this European material produced by European institutions

Reference

OJL 121 
Medicines for Human Use (Clinical Trials) Amendment Regulations 2006
Thursday, 20 July 2006
Statutory instruments
House of Lords
House of Commons
Medicines for Human Use (Marketing Authorisations etc.) Amendment Regulations 2008
Monday, 8 December 2008
Statutory instruments
House of Lords
House of Commons

EC documents

EC DRAFT 10607/97;EC DRAFT 7720/99;Dir2001/20/EC;

Published by

Not specified
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