1. M4 organization of the Common Technical Document for the Registration of Pharmaceuticals for Human Use Publication: Silver Spring, MD : Center for Drug Evaluation and Research, October 2017 Subject(s): Documentation -- standardsDrug ApprovalCongresses as TopicEuropean UnionInternational CooperationPharmaceutical Preparations -- standardsHumansCanadaEuropeJapanSwitzerlandUnited StatesUnited States. Department of Health and Human Services.United States. Food and Drug Administration.
