Medicines for Human Use (Clinical Trials) Regulations
Bulletin of Medical Ethics 2004 December-2005 January; (204): 2
Showing items related by title, author, creator and subject.
Draft Guidance on Consent by a Legal Representative on Behalf of a Person Not Able to Consent Under the Medicines for Human Use (Clinical Trials) Regulations 2003 Unknown author (Great Britain. Department of Health; Medicines and Healthcare Products Regulatory Agency (Great Britain), 2003-03)
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 Unknown author (European Union. European Parliament and Council of Europe, 2001-05-01)