FDA Compliance Actions Against IRBs and Clinical Investigators Paul W. Goebel, Jr., CIP Vice President [email protected] Chesapeake Research Review,
Wendy Lloyd BA, LPN, CIP,CCRP Regulatory Affairs and Compliance Specialist.
Informed Consent Philosophy 2803 Lecture IV Feb. 5, 2003.
BUILDING INFORMED CONSENT FOR PESTICIDE HANDLERS IN WASHINGTON Karl F. Weyrauch MD MPH Family Physician Research Consultant UW PNASH Member, Western Institutional.
Informed consent
1 Choice and Autonomy Ethical Issues in Women’s Health Meredith Schwartz Dalhousie University, Department of Philosophy.
Northeast Ethics Education Partnership (NEEP) Training Resources To access NEEP’s training materials, please visit
Ethical Principles for Biomedical Research Involving Human Subjects: Overview of International Guidelines Maria Fidelis C. Manalo, MD, MSc Epidemiology.
Use of a Short Form For inclusion of non-English speaking participants in human subject research * To play the presentation, click on the icon on the.
HUMAN RIGHTS REGULATION TRAINING Participation in Decision-Making Dana Martin Johnson, AAG The Institute of Law, Psychiatry, and Public Policy.
Medical Decision Making Nuala Kenny SC, OC, MD, FRCP Department of Bioethics (post-rtd) Dalhousie University, Halifax, NS Ethics & Health Policy Advisor.
Using the short form and reporting adverse events Erin Coons, Senior IRB Specialist, COMIRB 1.
