Due to the sheer scope and complexity of a clinical trial, guaranteeing your organization’s trial master file is contemporaneous and inspection ready is not a one-and-done deal. It’s a continuous and challenging process that requires management of many moving parts – across internal and external stakeholders. Join us and conquer the challenge at the Fierce TMF Summit on March 18-20 in Savannah, GA. Here's why you can't miss it: - Actionable insights: Industry veterans share battle-tested strategies through real-world case studies and interactive workshops.
- Expert guidance: Renowned TMF leaders answer your burning questions and help you optimize your processes.
- Powerful connections: Network with colleagues and build supportive relationships for future wins.
Register now and save $300 with our Best Rate. Prices increase after Friday, February 23rd. |
Panel: Strategies and Lessons Learned From Regulatory Inspections Workshop: TMF Inspection Readiness Essentials: Understanding Document Lifecycles, Translations, Regulatory Expectations, and Reducing Risk - Gillian Gittens, Director, e-Clinical Strategy & Solutions, TransPerfect Life Sciences
- Laurel-Ann Schrader, Director, Client Solutions, TransPerfect Life Sciences
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