This 20-page white paper provides a comprehensive, but accessible, overview of requirements and recommendations related to the 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.
Fill out the form below to download the Biopharma Process Analytical Technology White Paper.
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