Developing Monitoring Plans for Investigator-Initiated Clinical Trials

Tuesday, November 14, 2017 - 11:00am to 12:00pm

Albert Eye Research Institute Auditorium

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Presenter

Sandra SAM Sather, MS, BSN, CCRA, CCRC

Details

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

Nagorski, Susan
919-668-0502
susan.nagorski@dm.duke.edu

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