Reguatory Considerations for CMC & Assay Development of Live Biotherapeutics | Kisaco Research

Establishing an early-stage vision for bioprocessing developments of live biotherapeutic products from a datacentric perspective

  • Understanding the optimum CMC and understanding assay appropriateness for specific live biotherapeutic formulas.
  • Applying a targeted approach for CMC and assay development that reflects the regulatory landscape
  • The importance of integrating technical expertise and regulatory understanding
Speaker(s): 
Speakers

Author:

Mary Poor

Vice President of Quality and CMC
Siolta Therapeutics

Mary Poor

Vice President of Quality and CMC
Siolta Therapeutics