How to Develop PAT Approach-Regulatory Compliance 2015 is a webinar that covers topics such as:
- Regulatory impact of implementing PAT approach in R&D and production
- The fundamental concepts behind the FDA PAT initiative
- Efficient on-line and at-line tools for predicting quality attributes based on process data
- Use of multivariate data analysis (MVDA) and statistical process control
- Tools for root cause determination, trending analysis and visualization
- Design space verification and real time quality assurance
How to Develop PAT Approach-Regulatory Compliance 2015 is intended for:
- Process engineers
- Formulators
- Quality assurance personnel
- Validation specialists
- Anyone involved in risk mitigation and regulatory compliance
- Production managers