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dc.contributor.authorUramis, Emmaen
dc.contributor.authorVesper, Jamesen
dc.contributor.authorMcEachran, Daveen
dc.contributor.authorKaligis, Bennyen
dc.contributor.authorGiosafatte, Eliseo dien
dc.contributor.authorMills, Darrylen
dc.contributor.authorLewis, Geoffen
dc.contributor.authorCapone, Barbaraen
dc.contributor.authorJahdav, Suresh Sen
dc.contributor.authorHaslov, Kaareen
dc.contributor.authorVadsholt, Thomasen
dc.contributor.authorWorld Health Organization. Dept. of Immunization, Vaccines and Biologicalsen
dc.date.accessioned2012-06-17T01:22:27Z
dc.date.available2012-06-17T01:22:27Z
dc.date.created2006en
dc.date.issued2006en
dc.identifier.govdocWHO/IVB/05.24en
dc.identifier.urihttp://www.who.int/iris/handle/10665/69396
dc.description"This guide is the result of cooperation between many colleagues and institutions. Ms Emma Uramis, BioCen, and Mr James Vesper, LearningPlus, prepared it for the Global Training Network, in collaboration with: Mr Dave McEachran, Aventis Pasteur Limited, Dr Benny Kaligis, BioFarma, Dr Eliseo Di Giosafatte, Chiron S.p.A., Dr Darryl Mills and Mr Geoff Lewis, CSL Limited, Ms Barbara Capone, GlaxoSmithKline, Dr Suresh S. Jahdav, Serum Institute of India Ltd, Dr Kaare Haslov and MSc Thomas Vadsholt"--Acknowledgementsen
dc.descriptionParts 1 & 2 were published with the document numbers, WHO/VSQ/97.01 and WHO/VSQ/97.02en
dc.descriptionWHO/IVB/05.24en
dc.descriptionvii, 135 p.en
dc.language.isoenen
dc.publisherGeneva : World Health Organizationen
dc.subject.meshVaccinesen
dc.subject.meshDrug industryen
dc.subject.meshQuality controlen
dc.subject.meshGuidelineen
dc.subject.otherPharmaceuticals and Biologicalsen
dc.titleA WHO guide to good manufacturing practice (‎GMP)‎ requirements. Pt. 3, Trainingen
dc.subject.meshqualifierstandards educationen
dc.subject.meshqualifiereducationen


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