SOP 16. REPORTING REQUIREMENTS FOR UNANTICIPATED PROBLEMS,

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Date: 2014-03-10 08:07:42 Clinical research Pharmacology Drug safety Pharmaceutical industry Adverse event Institutional review board Food and Drug Administration National Institutes of Health Adverse effect Medicine Health Research		SOP 16. REPORTING REQUIREMENTS FOR UNANTICIPATED PROBLEMS, Add to Reading List Source URL: ohsr.od.nih.gov Download Document from Source Website File Size: 1,09 MB Share Document on Facebook

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