Natika Calhoun

Senior Regulatory Consultant

Natika Calhoun is a regulatory Subject Matter Expert for cellular and viral gene therapy products, biological APIs, and antibody-drug conjugates, based in California. In her current role, she works directly with manufacturing sites and customers as a regulatory liaison to support expansions, technical writings, filings, and submission success for clinical and commercial biological products.

·

Watch on Demand! Regulatory Considerations, Use of Ancillary Materials in Biologics Nov 14th, 2023

Understanding regulatory expectations for ancillary/raw materials during development and early clinical phases can be challenging. Join in for a roadmap of current requirements, with a focus on Cell and Gene Therapies.

by Natika Calhoun October 17, 2023

Start typing and press enter to search

Scroll to Top

Start typing and press enter to search