First Page | Document Content | |
---|---|---|
Date: 2010-03-07 04:38:53Medical ethics Clinical research ethics Design of experiments Clinical research Human subject research Institutional review board Ethics committee Clinical trial Scientific misconduct Informed consent Public Responsibility in Medicine and Research Outline of ethics | Microsoft Word - FERCAP Newsletter - February 2010.docAdd to Reading ListSource URL: www.fercap-sidcer.orgDownload Document from Source WebsiteFile Size: 236,05 KBShare Document on Facebook |
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 |