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dc.contributor.authorChaloner-Larsson, Gillianen
dc.contributor.authorAnderson, Rogeren
dc.contributor.authorEgan, Aniken
dc.contributor.authorDa Fonseca Costa Filho, Manoel Antonioen
dc.contributor.authorGomez Herrera, Jorge Fen
dc.contributor.authorWorld Health Organization. Vaccine Supply and Quality Uniten
dc.coverage.spatialGeneva
dc.date.accessioned2012-06-16T23:48:52Z
dc.date.available2012-06-16T23:48:52Z
dc.date.created1999en
dc.date.issued1999en
dc.identifier.govdocWHO/VSQ/97.01en
dc.identifier.govdocWHO/VSQ/97.02en
dc.identifier.urihttps://iris.who.int/handle/10665/64465
dc.descriptionWHO/VSQ/97.01en
dc.descriptionWHO/VSQ/97.02en
dc.description2pts. in 2v.en
dc.language.isoenen
dc.language.isoruen
dc.language.isoesen
dc.publisherWorld Health Organization
dc.publisherWorld Health Organization
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 / written by Gillian Chaloner-Larsson, Roger Anderson, Anik Egan; in collaboration with Manoel Antonio da Fonseca Costa Filho, Jorge F. Gomez Herreraen
dc.subject.meshqualifierstandardsen
dc.subject.meshqualifiermethodsen
who.relation.languageVersion10665/89219
who.relation.languageVersion10665/89220
who.relation.languageVersion10665/68527en
who.relation.languageVersion10665/64975en


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