Kelly Nolan, MS

Senior Manager, Regulatory Affairs
Visterra, Inc

Kelly Nolan is a Regulatory Affairs Senior Manager at Visterra, Inc. She has a biochemistry background with 6 years of CMC experience in early development stage products for small biotechs. Her experience is in both biologics and gene therapy, covering a variety of therapeutic areas including rare disease, autoimmune, neurology, and oncology.

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