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Best Practices for Clinical Trials
March 16 @ 1:00 pm - 2:30 pm
Best Practices for Clinical Trials is a two-part virtual course that supplements the online CITI Good Clinical Practice (GCP) training UW-Madison offers and highlights key information for personnel involved in the conduct of clinical trials. The sessions will include live interactive instruction and cover FDA regulations, GCP, the informed consent process, proper study documentation, and the difference between clinical practice vs. clinical research. Attendees will have an opportunity to ask questions. Pre-registration required.
Target Audience: Research Coordinators working on drug/device/FDA regulated trials within their first year of training or those interested in a refresher on these topics.
When: The course will be offered in two 1.5 hour sessions to allow for questions and discussion on Tuesday, March 16 and on Thursday, March 18 from 1-2:30pm CT. Attendance at both sessions is required.
Registration: Email Rochelle Rannow at email@example.com by March 15 at noon. Please include your name, email address, title, department and NetID. You will then receive links to the two courses.
Instructors: Chris Roginski, CCRC, Research Program Manager, Clinical Research Office and Shari Zeldin, BS, CCRC, Compliance and Regulatory Officer, Department of Medicine.