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dc.contributor.authorWorld Health Organization
dc.date.accessioned2012-06-16T14:44:23Z
dc.date.available2012-06-16T14:44:23Z
dc.date.created2005en
dc.date.issued2005en
dc.identifier9241209321en
dc.identifier0512-3054en
dc.identifier.urihttp://www.who.int/iris/handle/10665/43278
dc.description137 p.en
dc.language.isoenen
dc.publisherGeneva : World Health Organizationen
dc.relation.ispartofseriesWHO technical report series ; 932en
dc.subject.meshBiological productsen
dc.subject.meshImmunologic factorsen
dc.subject.meshReagent kits, Diagnosticen
dc.subject.meshBlooden
dc.subject.meshReference standardsen
dc.subject.meshGuidelineen
dc.subject.otherPharmaceuticals and Biologicalsen
dc.titleWHO Expert Committee on Biological Standardization : fifty-fifth reporten
dc.subject.meshqualifierstandardsen


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