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fermer cette partie de la bibliothèquegood practices in production
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Titre: Good Manufacturing Practices for Biological Products. In: WHO Expert Committee on Biological Standardization. Forty-second Report. Geneva, World Health Organization, 1992 (WHO Technical Report Series, No. 822), Annex 1; and WHO Expert Committee on Specifications for Pharmaceutical Preparations. Thirty-second Report. Geneva, World Health Organization, 1993 (WHO Technical Report Series, No. 834), Annex 3
Sujets: Quality and Safety: Medicines > Blood Products and Related Biologicals
Quality and Safety: Medicines > Quality Assurance
An: 1992 Pages: 11
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Régions: Global
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Titre: Good Manufacturing Practices: Supplementary Guidelines for the Manufacture of Pharmaceutical Excipients. WHO Technical Report Series, No. 885, 1999, Annex 5
Sujets: Quality and Safety: Medicines > Quality Assurance
An: 1999 Pages: 22
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Titre: Guidelines on Good Manufacturing Practices for Radiopharmaceutical Products. WHO Technical Report Series, No. 908, 2003, Annex 3
Sujets: Quality and Safety: Medicines > Quality Assurance
An: 2003 Pages: 10
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Titre: Supplementary Guidelines on Good Manufacturing Practices for the Manufacture of Herbal Medicines. WHO Technical Report Series, No. 937, 2006, Annex 3
Sujets: Traditional Medicine > Traditional, Complementary and Herbal Medicine
Quality and Safety: Medicines > Quality Assurance
An: 2006 Pages: 22
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Titre: WHO Good Manufacturing Practices for Active Pharmaceutical Ingredients. WHO Technical Report Series, No. 957, 2010, Annex 2
Sujets: Quality and Safety: Medicines > Quality Assurance
An: 2010 Pages: 62
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Titre: WHO Good Manufacturing Practices for Pharmaceutical Products: Main Principles. WHO Technical Report Series, No. 961, 2011, Annex 3
Sujets: Quality and Safety: Medicines > Quality Assurance
Prequalification of Medicines > WHO-UNICEF-UN Project
An: 2011 Pages: 54
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Régions: Global
 

Dernière mise à jour: le 3 mai 2013