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Food and Drug Administration Pharmaceutical industry Clinical Data Management Drug safety Common Technical Document New Drug Application International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use Drug Master File Center for Biologics Evaluation and Research Clinical research Research Medicine | Guidance for Industry Submitting Marketing Applications According to the ICH-CTD Format —Add to Reading ListSource URL: www.fda.govDownload Document from Source WebsiteFile Size: 174,62 KBShare Document on Facebook |