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![]() Date: 2016-08-02 13:55:17Medical ethics Clinical research ethics Human subject research Clinical research Design of experiments Informed consent Institutional review board Consent Clinical trial Health Insurance Portability and Accountability Act Treaty | 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 |