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close this section of the librarymanufacturing standards
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Title: Good Manufacturing Practices: Supplementary Guidelines for the Manufacture of Pharmaceutical Excipients. WHO Technical Report Series, No. 885, 1999, Annex 5
Subjects: Quality and Safety: Medicines > Quality Assurance
Year: 1999 Pages: 22
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Regions: Global
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Title: Pharmaceutical Development of Multisource (Generic) Finished Pharmaceutical Products – Points to Consider. WHO Technical Report Series, No. 970, 2012, Annex 3
Subjects: Quality and Safety: Medicines > Quality Assurance
Prequalification of Medicines > WHO-UNICEF-UN Project
Year: 2012 Pages: 29
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Title: Supplementary Guidelines on Good Manufacturing Practices for the Manufacture of Herbal Medicines. WHO Technical Report Series, No. 937, 2006, Annex 3
Subjects: Traditional Medicine > Traditional, Complementary and Herbal Medicine
Quality and Safety: Medicines > Quality Assurance
Year: 2006 Pages: 22
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Last updated: May 3, 2013