SQA Webinar: Maintaining Your TMF in an Inspection Steady State
SQA Webinar: Maintaining Your TMF in an Inspection Steady State
This online webinar will be given via Zoom.
Presented by: Dawn Niccum, inSeption Group
Webinar Category: Compliance
Regulatory Area of Interest: GCP
Description:
The Trial Master File is a key deliverable in a clinical trial. The records in the TMF should support all key decision making, oversight and conduct of the trial. Organizations struggle to ensure their TMF always ready for an inspection ("inspection steady"). This webinar will discuss approaches QA can support to an ensure an "inspection steady" TMF.
RQAP Re-registration units approved: TBD
Please sign in, select "Register Myself," and Proceed to checkout.
After registering, you will receive an email confirmation with the Zoom link information within 1 business day.
Registration
Last day to register is 8/17/2026