How Trial Master File Management Is Transforming And What You Need To Do To Stay Ahead

By Blake Adams, Florence Healthcare

Laptop clinical trials iStock-653839742

The Trial Master File (TMF) is one of the most critical elements of a clinical trial, in fact, it is one of the first items any regulatory agency requests. Yet, many organizations don’t place the same importance on the TMF as they do on patient recruitment or data management.

Unfortunately, the failure to prioritize the TMF can leave sponsors and clinical research organizations (CROs) to appear disorganized, delay clinical trial completion, and, in the worst cases, fail at bringing treatments to market.

The Next Phase podcast host Blake Adams sits down with Sholeh Ehdaivand to discuss the Trial Master Files (TMF) and its pivotal role in the future of real-time collaboration between clinical research sites and sponsors.

Sholeh, president and CEO of LMK Clinical Research Consulting, founded LMK eight years ago to provide Trial Master File (TMF) document management services and help organizations streamline clinical trials by optimizing their people and processes.

access the Q&A!

Get unlimited access to:

Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue. X

Enter your credentials below to log in. Not yet a member of Clinical Leader? Subscribe today.

Subscribe to Clinical Leader X

Please enter your email address and create a password to access the full content, Or log in to your account to continue.


Subscribe to Clinical Leader