Draft Guidance on Consent by a Legal Representative on Behalf of a Person Not Able to Consent Under the Medicines for Human Use (Clinical Trials) Regulations 2003
London: Medicines and Healthcare Products Regulatory Agency 2003; 19p. [Online]. Available: http://www.mhra.gov.uk/inforesources/publications/mlx287/content. pdf [2004 December 8]
Showing items related by title, author, creator and subject.
Guidance for Industry: Gene Therapy Clinical Trials -- Observing Participants for Delayed Adverse Events: Draft Guidance Center for Biologics Evaluation and Research [CBER] (United States) (2005-08)