Join Your Peers in West Palm Beach for 3 Days of Learning, Networking & Fun!
#FierceTMF #TooMuchFun
Boost Internal & External Collaboration, eTMF Processes, Integrated Technology, and Inspection Readiness
To comply with regulatory requirements pertaining to clinical trials, every organization involved in a clinical trial must maintain and store certain documents, images, and content related to the trial in the Trial Master File (TMF).
The Fierce TMF Summit is the leading event for pharmaceutical and biotech professionals responsible for managing TMF and clinical research, working to achieve optimal quality control, ensuring inspection readiness, and streamlining operations and technology.
Who Should Attend
Life science professionals from pharmaceuticals, biotech, and medical device organizations with responsibilities in:
- Clinical Documentations
- Clinical Operations
- Clinical Technology
- Clinical Trial Management
- GCP
- Inspection Readiness
- Quality Compliance / Management / Assurance
- Risk Management
- Trial Master File
- Trial, Records, Document Management
