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dc.contributor.authorWorld Health Assembly, 57
dc.coverage.spatialGenevaen
dc.date.accessioned2012-02-06T13:28:53Z
dc.date.available2012-02-06T13:28:53Z
dc.date.issued2004
dc.identifier.govdocA57/15
dc.identifier.urihttps://apps.who.int/iris/handle/10665/20091
dc.descriptionWorld Health Assembly fifty-seventh session, provisional agenda item 12.12en
dc.language.isoenen
dc.publisherWorld Health Organizationen
dc.subjectPharmaceutical productsen
dc.subjectBlood safetyen
dc.subject.meshDrug Industryen
dc.subject.meshDrug Monitoringen
dc.subject.meshPharmaceutical Preparationsen
dc.subject.meshBlooden
dc.subject.meshBlood Substitutesen
dc.subject.meshCommerceen
dc.subject.meshInterinstitutional Relationsen
dc.titleQuality and safety of medicines: regulatory sysems: report by the Secretariaten
dc.typeGoverning body documentsen
dc.subject.meshqualifierstandardsen
dc.subject.meshqualifierlegislation and jurisprudenceen
who.relation.languageVersion10665/20750en
who.relation.languageVersion10665/22413en
who.relation.languageVersion10665/21235en
who.relation.languageVersion10665/22902en
who.relation.languageVersion10665/20909en


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