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
Mary Poor
Vice President of Quality and CMC
Siolta Therapeutics