Process Analytical Technology Program
The FDA’s Process Analytical Technology (PAT) initiative promotes improved process understanding by defining Critical Process Parameters (CPP) and monitoring these CPPs, either in-line or on-line. Processes can become more efficient, with reduced over-processing and greater product consistency. Gain productivity by instituting a PAT program that is simple, data rich, and low-risk.
Process Mass Spectrometry Gas Analysis:
- Track batch progress in real-time
- Pinpoint contamination and maximize visible cell mass to increase profits
- Reduce over-processing/waste
- Increase product consistency with fault-tolerant operation