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dc.description.abstractThis document comprises the requirements for the initial registration of medicines (marketing authorization) in the Americas, prepared by the Working Group on Medicines Registration of the Pan American Network on Drug Regulatory Harmonization (PANDRH). Its purpose is to provide requirements for establishing regulations and regulatory tools that will contribute to the harmonization process of medicines registration to ensuring the efficacy, quality and safety of medicines to be available in the countries of our Region.en_US
dc.relation.ispartofseriesPan American Network on Drug Regulatory Harmonization - PANDRH, Technical Document;10
dc.subjectPharmaceutical Servicesen_US
dc.subjectPharmacy Administrationen_US
dc.subjectLegislation, Pharmacyen_US
dc.subjectResearch Reporten_US
dc.titleRequirements for Medicines Registration in the Americasen_US
dc.title.alternativeRequisitos para el registro de medicamentos en las Américasen_US
dc.rights.holderPan American Health Organizationen_US
dc.contributor.corporatenamePan American Health Organizationen_US
paho.publisher.countryUnited Statesen_US
paho.publisher.cityWashington, D.Cen_US

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