FDA Compliance Actions Against IRBs and Clinical Investigators Paul W. Goebel, Jr., CIP Vice President [email protected] Chesapeake Research Review,
INFORMED CONSENT/ MEDICAL TREATMENT Principles of liberty, self- determination, and autonomy support requirements of informed consent.
Consent and Capacity LMCC Part 1 preparation Tabitha Rogers MD, MSW PGY 2 Psychiatry.
Preventing Problems in Human Subjects Research: Tips from the IRB Joan Doherty, JD & Dominic Chiarelli, JD featuring Stephanie Hamilton, BSN, Damon Jacobson,
Ethical/Legal Aspects of Consent to Investigation or Treatment March 17, 2003 ISD II – MSK Barbara Barrowman Andrew Latus.
Research Compliance Office Consent Form Workshop Kristin B. Frazier HRPP Education Specialist Research Compliance Office January 24, 2008.
Part 1 of 3 Part Series: Informed Consent: The Document Wendy Lloyd, BA, LPN, CIP, CCRP Regulatory Affairs and Compliance Specialist Process Improvement.
Using the Internet to Conduct Research What Investigators and IRB Members Should Know -- January 29, 2009 -- Lisa Shickle, MS Analyst, VCU Massey Cancer.
FDA Compliance Actions Against IRBs and Clinical Investigators
Part 2 of 3 part series: Informed consent: The Process
Informed Consent Booklet
health information protection act.regulations-canada
