<--- Back to Details
| First Page | Document Content | |
|---|---|---|
 Date: 2016-02-04 11:59:13Accountability Medical research Administration Public records Ethics Design of experiments Clinical research ethics Pharmaceutical industry Institutional review board Records management Food and Drug Administration Grant |
Add to Reading List |
Institutional Review Board . ... . . | 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 |