CTSI 2025 FDA Symposium

Captain Kavita Dada, PharmD, RAC, Associate Director for Regulatory Operations with the FDA Center for Drug Evaluation and Research, will provide the keynote address. 

The symposium will feature a series of insightful sessions aimed at exploring FDA-regulated research guidelines, discussing the evolving drug and device development regulatory processes and applying quality improvement approaches to enhance inspection readiness in clinical trials. Attendees will gain valuable insights into the latest innovations in FDA-regulated clinical trials, enhance their understanding of regulatory processes and hear from industry experts. A lunch will be provided.