French Nutrition and Health Survey 2006 - 2007 (Etude Nationale Nutrition Santé ENNS 2006 – 2007) French Institute for Public Health Surveillance.
New IRB Policies Reporting Unanticipated Problems & Adverse Events Data & Safety Monitoring Susan Burner Bankowski, M.S., J.D. Chair, OHSU IRB.
COMMON PROBLEMS IN INFORMED CONSENT Jeri R. Barney, JD, MS Michele Antisdel, MBA/CCRP HRPP Compliance ManagerIRB Regulatory Analyst Human Research Protection.
Ny Presbyterian Quality Symposium
Cox Regression
Medical Billing Compliance Clinical Trial Billing Audits at Yale: Processes and Findings November 10, 2011.
INFORMED CONSENT: PROCESS, DOCUMENTATION, ALTERATION AND WAIVERS Suzanne Sparrow.
Research Ethics The American Psychological Association Guidelines Protecting the Welfare of Animal Subjects Fraud in Science Plagiarism Ethical Reports.
Columbia University Medical Center Research Billing Compliance presented by Office for Billing Compliance Research Billing Compliance presented by Office.
1 Writing Better Consent Forms Rick Wagner Associate Director Human Research Protection Program [email protected] .
Adverse Events, Unanticipated Problems, Protocol Deviations & other Safety Information Which Form 4 to Use?
1 Clinical Trials. 2 This is part of drug registration but may be purely scientific: part of international multicentre trials for sponsors In the legislation.
