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

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: 1 GCP | non-GLP | non-GMP