Tulay Kilicdagi, MA, RAC-Drugs

Associate Director, Regulatory Affairs
Visterra, Inc

Tulay Kilicdagi is working as Regulatory Affairs Assoc. Director at Visterra, Inc., a biologics research and early-stage clinical development company based in Waltham, Massachusetts. As a member of the Visterra Regulatory Affairs department she is currently leading a monoclonal antibody program, responsible for building the regulatory development plan and managing Health Authority interactions and submissions. She is also leading regulatory document management systems and tools at Visterra.

Presentation(s):

• CDER’s Product Quality Review of Biologics & Biosimilars: Common Findings, Review Issues and Post-Marketing Recommendations

  Wednesday, September 18, 2024
  1:00 PM - 2:00 PM PDT