Developing Monitoring Plans for Investigator-Initiated Clinical Trials
Tuesday, November 14, 2017
11:00 am - 12:00 pm
Albert Eye Research Institute Auditorium
Sandra SAM Sather, MS, BSN, CCRA, CCRC
This presentation will cover the requirements and best practices of establishing, maintaining, and complying with a study monitoring plan for investigator-initiated trials. Join us for this session and go through a real life case example of where adequate monitoring plans can support investigator-initiated trial success.