<--- Back to Details
| First Page | Document Content | |
|---|---|---|
 Date: 2012-06-04 10:01:36Medical ethics Clinical research ethics Professional ethics Human subject research Research ethics Institutional review board Ethics Informed consent Outline of ethics Research ethics consultation |
Add to Reading List |
DRAFTNovember 2011 Standard Operating Procedure Research Ethics Committee: | 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 |