Show simple item record

dc.contributor.authorWorld Health Organization. Division of Drug Management and Policiesen
dc.coverage.spatialGeneva
dc.date.accessioned2012-06-16T23:26:12Z
dc.date.available2012-06-16T23:26:12Z
dc.date.created1996en
dc.date.issued1996en
dc.identifier.govdocWHO/PHARM/96.588en
dc.identifier.urihttp://www.who.int/iris/handle/10665/63173
dc.descriptionONLINEen
dc.descriptionWHO/PHARM/96.588en
dc.description5 p.en
dc.language.isoenen
dc.publisherWorld Health Organization
dc.publisherWorld Health Organization
dc.subject.meshDrug industryen
dc.subject.meshQuality controlen
dc.subject.meshGuidelineen
dc.subject.otherPharmaceuticals and Biologicalsen
dc.titleGood manufacturing practices : authorized person : the role, functions and trainingen
dc.subject.meshqualifierstandards manpoweren


Files in this item

Thumbnail

This item appears in the following Collection(‎s)‎

Show simple item record