Coordinator Webinar Series

As a Senior Project Manager and Regulatory Document Specialist at the Center for Health + Technology (CHeT), Becky has been involved in and responsible for the management and health of the Trial Master Files (TMF) for many multi-site studies in the field of therapeutic clinical research. Working closely with site staff, monitors, sponsors, and study team members, Becky serves as a Subject Matter Expert (SME) for the regulatory aspects of a study. Within CHeT, Becky also serves as a leading member of the Regulatory Management Group, and serves as an SME for electronic TMF (eTMF) systems.

Becky Gravenstede, BA

Center for Health + Technology

Regulatory Basics

Recorded on November 10, 2022