Developing Monitoring Plans for Investigator-Initiated Clinical Trials
Tuesday, November 14, 2017
11:00 am - 12:00 pm
Sandra SAM Sather, MS, BSN, CCRA, CCRC
Sponsor(s): School of Medicine - Regulatory Affairs, Department of Surgery, Duke Center for Applied Genomics and Precision Medicine, Duke Clinical and Translational Science Institute (CTSI), Duke Clinical Research Institute (DCRI), Duke Office of Clinical Research (DOCR), MEDx, School of Medicine (SOM), and School of Nursing (SON)
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.
Contact: Susan Nagorski
