Slide 11 Prompt Reporting for Investigators and Research Staff Conducting Research, IRBs 1, 2, and 3 University of Illinois at Chicago Office for the Protection of Research…

Slide 1FLYING SAMS AT UCSD WINTER WEEK 3 GBM Jan 23 2013 http://ucsdflyingsams.com Slide 2 Clinic updates December 15th Fiesta Clinic w Dr. Obryan Saw Dental patients with…

Slide 1Understanding Research: Getting Your Project Ready for the IRB Jill Stoltzfus, Ph.D. Director, Research Institute [email protected] Slide 2 Todays Objectives Present…

Slide 1FDA Regulation of Pharmaceuticals and Devices Jean Toth-Allen, Ph.D. Good Clinical Practice Program Office of Science and Health Coordination Office of the Commissioner…

Slide 1Regulation of Medical Devices Celia M. Witten, Ph.D., M.D. Director Division of General, Restorative and Neurological Devices Office of Device Evaluation Food and…

Slide 1 Slide 2 What is HIPAA ? HIPAA with the DHPG Research Medical Records Clinical Trials Business Associate Agreement Michael Shoob, Elizabeth BankertFebruary 2003 Slide…

Slide 1USC Clinical Trials Office (CTO) Submitting your Studies to CTO For Processing Soheil Jadali Director, Clinical Trial Office Slide 2 Clinical Trials Office (CTO) CTO…

Slide 1Introduction to Research Pharmacy Investigational Drug Control and Patient Safety CUMC RP Robert B. MacArthur, Pharm.D. Slide 2 “ Why does it take so long and cost…

Slide 1Is it Research? Slide 2 Is It Research? 2 Elements –The project involves a systematic investigation –The design (meaning goal, purpose, or intent) of the investigation…

Slide 1Food and Drug Administration Center for Biologics Evaluation and Research The Office of Cellular, Tissue, and Gene Therapies Web Seminar Series presents: The Office…