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dc.contributor.authorWorld Health Organization. Division of Drug Management and Policiesen
dc.coverage.spatialGeneva
dc.date.accessioned2012-06-16T22:34:33Z
dc.date.available2012-06-16T22:34:33Z
dc.date.created1993en
dc.date.issued1993en
dc.identifier.govdocWHO/PHARM/93.561. Unpublisheden
dc.identifier.urihttps://iris.who.int/handle/10665/60010
dc.descriptionONLINEen
dc.descriptionWHO/PHARM/93.561. Unpublisheden
dc.description5 p.en
dc.language.isoenen
dc.publisherWorld Health Organization
dc.publisherWorld Health Organization
dc.subject.meshHerbal Medicineen
dc.subject.meshPlants, Medicinalen
dc.subject.meshQuality Controlen
dc.subject.meshDrug Industryen
dc.subject.otherPharmaceuticals and Biologicalsen
dc.titleGood manufacturing practices for pharmaceutical products : supplementary guidelines for the manufacture of herbal medicinal productsen
dc.subject.meshqualifierstandardsen


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