Slide 1FDA Compliance Actions Against IRBs and Clinical Investigators Paul W. Goebel, Jr., CIP Vice President [email protected] Chesapeake Research Review, Inc. 410-884-2900…

Slide 1INFORMED CONSENT/ MEDICAL TREATMENT Principles of liberty, self- determination, and autonomy support requirements of informed consent. Slide 2 The Elements of Consent…

Slide 1Consent and Capacity LMCC Part 1 preparation Tabitha Rogers MD, MSW PGY 2 Psychiatry Slide 2 Objectives To review the different types of consent. To review the criteria…

Slide 1 Preventing Problems in Human Subjects Research: Tips from the IRB Joan Doherty, JD & Dominic Chiarelli, JD featuring Stephanie Hamilton, BSN, Damon Jacobson,…

Slide 1 Ethical/Legal Aspects of Consent to Investigation or Treatment March 17, 2003 ISD II – MSK Barbara Barrowman Andrew Latus Slide 2 Outline – Consent  General…

Slide 1 Research Compliance Office Consent Form Workshop Kristin B. Frazier HRPP Education Specialist Research Compliance Office January 24, 2008 Slide 2 Research Compliance…

Slide 1 Part 1 of 3 Part Series: Informed Consent: The Document Wendy Lloyd, BA, LPN, CIP, CCRP Regulatory Affairs and Compliance Specialist Process Improvement Team Slide…

Slide 1 Using the Internet to Conduct Research What Investigators and IRB Members Should Know -- January 29, 2009 -- Lisa Shickle, MS Analyst, VCU Massey Cancer Center Member…

FDA Compliance Actions Against IRBs and Clinical Investigators Paul W. Goebel, Jr., CIP Vice President [email protected] Chesapeake Research Review, Inc. 410-884-2900 www.chesapeakeirb.com…

Slide 1 Part 2 of 3 part series: Informed consent: The Process Wendy Lloyd BA, LPN, CIP,CCRP Regulatory Affairs and Compliance Specialist Objectives Identify consent process…