This 20-page white paper provides a comprehensive,
but accessible, overview of requirements and recommendations related to the U.S. FDA’s Process Analytical Technology (PAT) initiative for the biopharmaceutical industry.
- Understand critical process parameters (CPPs), critical quality attributes (CQAs), and key performance indicators (KPIs) for fermentation control in the bioreactor.
- Know which CPPs and KPIs are the most reliable to efficiently monitor your process.
- See the most recent examples of PAT applied in the biopharma industry and R&D.