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close this section of the libraryclinical trials in humans
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Title: Good Manufacturing Practices: Supplementary Guidelines for the Manufacture of Investigational Pharmaceutical Products for Clinical Trials in Humans. WHO Technical Report, Series No. 863 , 1996, Annex 7
Subjects: Quality and Safety: Medicines > Quality Assurance
Year: 1996 Pages: 16
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Regions: Global
 

Last updated: May 3, 2013