Process Analytical Technology (PAT): The Impact on Pharmaceuticals Manufacturing and Validation Needs/Requirements

This webinar will provide an insight into the practical aspects of Process Analytical Technology (PAT) and will be an invaluable source of information on various technologies and approaches that fit the PAT definitions. You will learn about regulatory initiatives to improve the quality of pharmaceutical manufacturing using PAT and validation thereof. No special technical background is required.

Areas Covered:-

This webinar course covers the following topics on Process Analytical Technology:

• What is FDA PAT Initiative and how to comply with innovation requirement
• FDA PAT Guidance Q&A with examples
• Multivariate data acquisition and analysis tools
• Modern process analyzers
• Process and endpoint monitoring and control tools
• Current GMP practices, QbD, and Risk-based PAT framework
• Life Cycle Validation approach applied to analytical technology

Who Should Attend:-

This webinar is intended for formulators, process engineers, validation specialists, and quality assurance personnel, as well as production managers occupied with process and product quality assurance. It will also provide a good source of information for anyone involved in risk mitigation and regulatory compliance.