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![]() Date: 2016-02-04 12:00:59Medical research Clinical research ethics Research Medical ethics Human subject research Clinical research Pharmaceutical industry Institutional review board Public Responsibility in Medicine and Research Informed consent Standard operating procedure Office for Human Research Protections | Add to Reading List |
![]() | Ethics and Clinical Trials in Resource Limited Settings George M. Carter, Director, Foundation for Integrative AIDS Research (FIAR), Brooklyn, NY, USADocID: 1usfj - View Document |
![]() | Community Advisory Groups: can they facilitate ethical research in clinical trials? Anant Bhan Independent Researcher- Bioethics and public health Member, Institutional Ethics Committee, University of PuneDocID: 1s3GI - View Document |
![]() | Microsoft Word - SOP - IRB Membership.docxDocID: 1rrOd - View Document |
![]() | Food and Drug Administration, HHS § 50.3 PART 50—PROTECTION OF HUMAN SUBJECTSDocID: 1rraL - View Document |
![]() | Microsoft Word - SOP editedonlineversibaru.docDocID: 1rqX4 - View Document |