First Page | Document Content | |
---|---|---|
![]() 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 | 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 |