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Date: 2015-07-01 12:45:56Clinical research ethics Medical research Ethics Research Design of experiments Drug safety Institutional review board Regulatory compliance Public Responsibility in Medicine and Research Office for Human Research Protections IRB Clinical research coordinator | Microsoft Word - SOP - IRB Membership.docxAdd to Reading ListSource URL: research.missouri.eduDownload Document from Source WebsiteFile Size: 29,31 KBShare Document on Facebook |
Regulatory Oversight through HRPP Melody Lin, Ph.D. Deputy Director, Office for Human Research Protections Director, International ActivitiesDocID: 1rJeK - View Document | |
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