A presentation on 8/23/2007 by Jean Toth-Allen, Ph.D., Good Clinical Practice Program
Office of Science and Health Coordination
Office of the Commissioner
Food and Drug Administration (FDA)
Doris Cook is Project Manager at the Ethics Office of the Canadian Institutes of Health Research (CIHR) and is working on the development of the CIHR Guidelines for Health Research Involving Aboriginal Peoples. Doris Cook
Jonathan Moreno, PhD; Arthur L. Caplan, PhD; Paul Root Wolpe, PhD; and the Members of the Project on Informed Consent, Human Research Ethics Group.
JAMA. 1998;280:1951-1958.
In order to qualify for an Assurance, the OHRP strongly recommends that the Institutional Official complete Module 1. The Human Protections Administrator (Primary Contact) and IRB Chair should complete all three modules.
IRB Teaching Guide
Protecting Human Research Subjects. A Guide for Student Investigators
Are You Conducting Research Using Human Subjects? A Guide for Principal Investigators
Reportable Events Lecture Presented By CHLA
Violating the Rights and Welfare of Research Subjects Presented By CHLA
Retrospective Studies and Case Reports Presented By CHLA
Is Your Project Human Subjects Research? A Guide for Investigators
Tip Sheets
Glossary
Jointly sponsored by:
Community-Campus Partnerships for Health (CCPH) and the Tuskegee University National Center for Bioethics in Research and Health Care (the Bioethics Center)