First Page | Document Content | |
---|---|---|
Date: 2016-04-12 01:21:57Medical research Research Medical ethics Health Clinical research ethics Clinical research Design of experiments Pharmaceutical industry Clinical trial Institutional review board Informed consent Consent | Add to Reading ListSource URL: humansubjects.stanford.eduDownload Document from Source WebsiteFile Size: 146,50 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 |