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Date: 2014-01-30 11:37:23Medical research Research Clinical research Medical ethics Pharmaceutical industry Food and Drug Administration Investigational device exemption Clinical trial Institutional review board Informed consent Clinical investigator Human subject research | Food and Drug Administration, HHS § 50.3 PART 50—PROTECTION OF HUMAN SUBJECTSAdd to Reading ListSource URL: publicfiles.jaeb.orgDownload Document from Source WebsiteFile Size: 203,47 KBShare Document on Facebook |