Draft Guidance on Consent by a Legal Representative on Behalf of a Person Not Able to Consent Under the Medicines for Human Use (Clinical Trials) Regulations 2003

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Unknown author
Bibliographic Citation
London: Medicines and Healthcare Products Regulatory Agency 2003; 19p. [Online]. Available: http://www.mhra.gov.uk/inforesources/publications/mlx287/content. pdf [2004 December 8]
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http://hdl.handle.net/10822/1001878
Date
2003-03
Subject
Publisher
Great Britain. Department of Health; Medicines and Healthcare Products Regulatory Agency (Great Britain)
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