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dc.contributor.authorWorld Health Organization
dc.coverage.spatialGenevaen_US
dc.date.accessioned2016-12-09T15:47:31Z
dc.date.available2016-12-09T15:47:31Z
dc.date.issued2016
dc.identifier.govdocWHO/EMP/RHT/PQT/2016.01
dc.identifier.urihttps://iris.who.int/handle/10665/251915
dc.description27 p.en_US
dc.language.isoenen_US
dc.publisherWorld Health Organizationen_US
dc.rightsCC BY-NC-SA 3.0 IGO
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/3.0/igo/
dc.subject.meshQuality Controlen_US
dc.subject.meshIn Vitro Techniquesen_US
dc.subject.meshEquipment and Suppliesen_US
dc.titleReportable changes to a WHO prequalified in vitro diagnostic medical deviceen_US
dc.typeTechnical documentsen_US
dc.rights.holderWorld Health Organization


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