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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
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Document Date: 2014-01-30 11:37:23

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File Size: 203,47 KB

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