Trial Master File (TMF) for Research Sites: Set-Up and Maintenance
Sign up to be notified of new teleseminars daily! |
Description: | This clinical compliance webinar will discuss the elements of a Trial Master File (TMF) and show how to set-up and maintain the TMF to ensure it can pass inspection by a clinical trial monitor or auditor. Why Should You Attend: - How would you handle missing elements of a regulatory file? - Who is responsible for which essential elements in a TMF? - How do you handle versioning of protocols in a TMF? This course will go over the essential documents which make up the Trial Master File. The presenter will help you understand the fundamentals of the set-up and maintenance of the TMF so you can ensure that when a monitor or auditor visits, the appropriate documentation will be easily located and you will be assured that you have all the documentation required. Areas Covered in the Webinar: - ICH guidelines and Good Clinical Practice (GCP) - Organization of the TMF - How to write good Memos for TMF - Versioning in a TMF - Access and control of the TMF - Staff responsibilities of the TMF - Long term storage of the TMF |
URL: | http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=703012?channel=telesemin |
Date: | Friday, July 19, 2013 |
Time: | 2:00pm-3:00pm UTC |
Duration: | 1 hour |
Access: | Public |
Category: | Webinar*, Health* |
Created by: | Public Access |
Updated: | Thursday, July 11, 2013 7:12am UTC |
: | $199 |
: | +1-650-620-3915 |
: | referral@complianceonline.com |
: | Referral |
: | +1-650-620-3915 |
Comments: | None |