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Medicine / Science / Design of experiments / Pharmacology / Drug safety / Institutional review board / Investigational Device Exemption / National Institutes of Health / Public Responsibility in Medicine and Research / Clinical research / Research / Pharmaceutical industry


SOP 4 Human Research Protection Program (HRPP) Documentation and Records
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Document Date: 2014-03-10 08:08:26


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File Size: 244,75 KB

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IndustryTerm

deferred protocols / /

Organization

FDA / NIH IRB / National Institute of Health / Data Safety and Monitoring Board / Food and Drug Administration / G. Institute / International Rugby Board / IRB ADMINISTRATIVE OFFICE / Convened NIH Institutional Review Board / office of Human Subjects Research Protections / IRB / /

Person

Involving Adults / /

Position

Investigator / Chair / contractor / Institutional Official / General / /

PublishedMedium

the Conduct of Research Review / the Ethical and Regulatory Review / /

Technology

10 4.6 RESEARCH PROTOCOL / previously deferred protocols / research protocol / 3.3 IRB RESEARCH PROTOCOL FILES A. All Protocols / 3.3 IRB RESEARCH PROTOCOL / /

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