GET THE ULTIMATE CLINICAL TRIAL TRACKING CHECKLIST
In this webinar, Gill Gittens and Laurel-Ann Schrader discuss key takeaways from the CDISC + TMF Europe Interchange. This session brings together insights from some of the top minds in clinical operations, as they discuss the evolving expectations in Trial Master File (TMF) management and how global regulatory alignment is reshaping best practices.
From building resilient inspection-readiness cultures to addressing the practical challenges of eTMF adoption, our speakers will share frontline observations and forward-looking strategies to help TMF professionals keep pace with a complex and rapidly changing environment.
What you’ll learn:
• How to align TMF practices with the latest global guidance, including ICH E6(R3)
• Ways to strengthen collaboration between sponsors and CROs through effective oversight models
• Key themes and lessons from the CDISC TMF Europe Interchange discussions
Whether you're a sponsor, CRO, or TMF professional navigating oversight and compliance, this is your opportunity to gain timely insights from those driving transformation in the TMF space.
Gill Gittens
Director, e-Clinical Strategy & Solutions
Laurel-Ann Schrader
Director, Client Solutions