<--- Back to Details
First PageDocument Content
Medical research / Applied ethics / Medical ethics / Clinical research ethics / Research / Human subject research / Clinical research / Design of experiments / Institutional review board / Public Responsibility in Medicine and Research / Informed consent / Clinical research coordinator
Medical research
Applied ethics
Medical ethics
Clinical research ethics
Research
Human subject research
Clinical research
Design of experiments
Institutional review board
Public Responsibility in Medicine and Research
Informed consent
Clinical research coordinator

American Public University System March 2016 Institutional Review Board

Add to Reading List

Source URL: www.apus.edu

Download Document from Source Website

File Size: 302,00 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

DocID: 1s3GI - View Document

Clinical research ethics / Medical research / Ethics / Research / Design of experiments / Drug safety / Institutional review board / Regulatory compliance / Public Responsibility in Medicine and Research / Office for Human Research Protections / IRB / Clinical research coordinator

Microsoft Word - SOP - IRB Membership.docx

DocID: 1rrOd - View Document

Medical research / Research / Clinical research / Medical ethics / Pharmaceutical industry / Food and Drug Administration / Investigational device exemption / Clinical trial / Institutional review board / Informed consent / Clinical investigator / Human subject research

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

DocID: 1rraL - View Document

Medical research / Clinical research / Pharmaceutical industry / Institutional review board / Clinical trial / Good clinical practice / Informed consent / Adverse event / Protocol / Ethics committee / Serious adverse event / University Malaya Medical Centre

Microsoft Word - SOP editedonlineversibaru.doc

DocID: 1rqX4 - View Document