<--- Back to Details
First PageDocument Content
Medical research / Medical ethics / Clinical research ethics / Autonomy / Applied ethics / Research / Human subject research / Clinical trials / Informed consent / Consent / Title 1 of the Code of Federal Regulations
Date: 2016-04-12 01:21:51
Medical research
Medical ethics
Clinical research ethics
Autonomy
Applied ethics
Research
Human subject research
Clinical trials
Informed consent
Consent
Title 1 of the Code of Federal Regulations

CHK-3m IRB MEDical Reviewer Checklist FORM

Add to Reading List

Source URL: humansubjects.stanford.edu

Download Document from Source Website

File Size: 87,50 KB

Share Document on Facebook

Similar Documents

Building Sustainable Services through Brief International Projects: The Ethics of International Medical Trips

DocID: 1vrjM - View Document

S.C. Board of Veterinary Medical Examiners Information for Practitioners As a reminder, you are required to comply with the Principles of Veterinary Medical Ethics of the AVMA, pursuant to S.C. Code Ann. § A)(

DocID: 1vlZE - View Document

Awareness about Knowledge, Attitude and Practice of Medical Ethics pertaining to Patient Care, among Male and Female Physicians Working in a Public Sector Hospital of Karachi, Pakistan - A Cross-Sectional Survey

DocID: 1veD6 - View Document

© FICEM FebruaryFederative International Committee for Ethics and Medical Humanities (FICEM) of the International Federation of Associations of Anatomists (IFAA) Thomas H. Champney / USA, Jon Cornwall / New Zeala

DocID: 1vckS - View Document

Workshop Program 5th ICMM Workshop on Military Medical Ethics 07 – 09 May 2015 – Forum Lilienberg Ermatingen, Switzerland

DocID: 1vapP - View Document