Food and Drug Administration, HHS § 50.3 PART 50—PROTECTION OF HUMAN SUBJECTS

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Date: 2014-01-30 11:37:23 Medical 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 SUBJECTS Add to Reading List Source URL: publicfiles.jaeb.org Download Document from Source Website File Size: 203,47 KB Share Document on Facebook

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