Back to Agenda
Improving Trial Quality by Better Preparing Site Teams
Session Chair(s)
Sabrina Comic-Savic, MD, MPH
Vice President, Quality Assurance, Clinical Project Oversight
Novartis, United States
This session will describe new CTTI recommendations that provide a pathway for: Implementing a more efficient and effective means of investigator qualification, determining whether a site team is a good fit for a particular protocol, and improving the understanding of how to apply GCP principles to the conduct of clinical trials.
Learning Objective : Identify the limitations of current approaches to preparing investigators for conducting clinical trials; Describe strategies for eliminating the distinction between the “qualifying” and “preparing” investigators; Implement actionable recommendations to support a more fit-for-purpose, risk-based, and streamlined approach to investigator requirements.
Speaker(s)
Panelist
Christine Marie Hildebrand
Amici, United States
Physician Assistant, Sub-Investigator, Clinical Operations Lead
Panelist
Jimmy Bechtel, MBA
Society for Clinical Research Sites (SCRS), United States
Vice President, Site Engagement
Industry Update
Janette Panhuis, BSN, MBA, RN
PHRI, Canada
Consultant
Veronica Todaro, MPH
Parkinson's Foundation, United States
Chief Operating Officer
Have an account?