<--- Back to Details
First PageDocument Content
Medical research / Clinical research ethics / Research / Applied ethics / Medical ethics / Clinical research / Research ethics / Institutional review board / Regulatory compliance / Human subject research / Food and Drug Administration / Medical device
Date: 2014-06-04 09:40:57
Medical research
Clinical research ethics
Research
Applied ethics
Medical ethics
Clinical research
Research ethics
Institutional review board
Regulatory compliance
Human subject research
Food and Drug Administration
Medical device

HRPP GUIDELINE 202 Determination of Human Subjects Research Issuing Office: Office of Research Administration

Add to Reading List

Source URL: www.irb.purdue.edu

Download Document from Source Website

File Size: 128,76 KB

Share Document on Facebook

Similar Documents

Ethics and Clinical Trials in Resource Limited Settings George M. Carter, Director, Foundation for Integrative AIDS Research (FIAR), Brooklyn, NY, USA

DocID: 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 Pune

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 Pune

DocID: 1s3GI - View Document

Microsoft Word - SOP - IRB Membership.docx

Microsoft Word - SOP - IRB Membership.docx

DocID: 1rrOd - View Document

Food and Drug Administration, HHS  § 50.3 PART 50—PROTECTION OF HUMAN SUBJECTS

Food and Drug Administration, HHS § 50.3 PART 50—PROTECTION OF HUMAN SUBJECTS

DocID: 1rraL - View Document

Microsoft Word - SOP editedonlineversibaru.doc

Microsoft Word - SOP editedonlineversibaru.doc

DocID: 1rqX4 - View Document