The eTMF As A Regulatory Standard
Source: TransPerfect
Join Gillian Gittens and Laurel-Ann Schrader as they delve into ICH GCP Essential Documents and the regulatory landscape surrounding Trial Master File (TMF) requirements to ensure high quality throughout a clinical trial.
By watching this webinar, viewers will gain essential insights on regulatory guidance and how an eTMF can improve your existing TMF, such as:
- Structure
- Security
- Quality
- Scanning
- Archiving
- Compliance & Validation
access the Webinar!
Log In
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 Tech Leader? Subscribe today.
Subscribe to Clinical Tech Leader
X
Subscribe to Clinical Tech Leader
This website uses cookies to ensure you get the best experience on our website. Learn more