Developing Monitoring Plans for Investigator-Initiated Clinical Trials

Nov 14

Tuesday, November 14, 2017

11:00 am - 12:00 pm
Albert Eye Research Institute Auditorium

Presenter

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.

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Contact

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

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