Guidance for Industry: Protecting the Rights, Safety, and Welfare of Study Subjects - Supervisory Responsibilities of Investigators - Trial practice - Document - PDFSEARCH.IO

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Pharmaceutical sciences Pharmacology Design of experiments Clinical trial Clinical investigator Institutional review board Food and Drug Administration Good Clinical Practice Regulatory requirement Clinical research Research Pharmaceutical industry		Guidance for Industry: Protecting the Rights, Safety, and Welfare of Study Subjects - Supervisory Responsibilities of Investigators Add to Reading List Source URL: www.fda.gov Download Document from Source Website File Size: 134,07 KB Share Document on Facebook

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