Oversight of Clinical Investigations: A RiskBased Approach to Monitoring (Draft Guidance) U.S. Department of Health and Human Services Food and Drug Administration Center for Biologics Evaluatio

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Pharmaceutical industry Pharmacology Food and Drug Administration Clinical trial Clinical investigator Regulatory requirement Good Clinical Practice Center for Drug Evaluation and Research Good Clinical Data Management Practice Clinical research Research Pharmaceutical sciences		Oversight of Clinical Investigations: A RiskBased Approach to Monitoring (Draft Guidance) U.S. Department of Health and Human Services Food and Drug Administration Center for Biologics Evaluatio Add to Reading List Source URL: www.fda.gov. Download Document from Source Website File Size: 525,67 KB Share Document on Facebook

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