The Trial Master File (TMF) is the repository for all essential documents supporting a clinical trial. But its role is going beyond a simple storage container for files, as CROs and Sponsors work together to manage the collection of TMF documents and the review and inspection processes, both internally and externally.
Join Agatha and DZS Clinical Services on February 17th, at 1 pm ET (10 am PT), when they will discuss how clinical trial sponsors and CROs can leverage a shared electronic TMF as a hub for collaboration and coordination of the TMF.
During the webinar, Agatha’s Head of North American Operations, Ken Lownie, and Kari Brown, Director of Clinical Operations, DZS Clinical Services, will discuss:
• The role of the TMF and how it is evolving
• Why CROs and Sponsors need to work together to manage the TMF successfully
• How the right eTMF enforces process coordination and collaboration
• The key features of a modern eTMF application
• How to build a shared responsibility model for the TMF
Whether you are a CRO looking for a way to work more efficiently with your sponsors or a sponsor looking for an eTMF that your team and your CROs can use, this webinar will be packed with helpful information to guide your decision.
|
