Trial Master File (TMF): FDA Expectations from Sponsors and Sites 2017
24 Feb 2017
Webinar
Description
Topics
Required components of a TMF
FDA’s expectation from site and sponsor’s documents
Electronic and Paper TMF requirements
Best practices for the set-up and maintenance of TMF
Common errors in TMF management
Who should Attend
Clinical Research Coordinators (CRCs)
Clinical Research Associates (CRAs)
Principal Investigators
Clinical Research Administrators
Sponsors of INDs
Project Managers
People investing in FDA-regulated product development projects
Past Events
Trial Master File (TMF): FDA Expectations from Sponsors and Sites 2017 - 24 Feb 2017, Webinar (40454)
Important
Please, check "Trial Master File (TMF): FDA Expectations from Sponsors and Sites" official website for possible changes, before making any traveling arrangements
Event Categories
Government & Global Issues: Law & Regulations
Health & Medicine: Medical laboratories, Medical technology
