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 Christina Allen, Associate Director, TMF Operations, Daiichi Sankyo MCKenzie Beets, Senior Manager, Clinical Document Management, Takeda Donna Dorozinsky, Founder & CEO, Just in Time GCP Liz Farrell, Director, Trial Master File, Agios Pharmaceuticals Cristina Monastero, Associate Director, Clinical Document Management, Larimar TherapeuticsFiona Wallace, Senior Manager, TMF Operations, Alnylam 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 |