Trial Master File (TMF): FDA Expectations from Sponsors and Sites 2017 is a webinar that covers topics such as:
- 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
Trial Master File (TMF): FDA Expectations from Sponsors and Sites 2017 is intended for:
- 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
