Cleaning Validation - Regulatory Expectations

This training session will help to understand what is cleaning validation, why cleaning validation is important. This session will take you through some examples of FDA citations, regulatory agencies requirements, role of quality risk management in cleaning validation, finding worst case limit, LOD , LOQ and recovery study concepts, Surviving audits with the aspect of cleaning validation, Handling of new product introduction in manufacturing plant and inspection readiness. Finally the session will end with Q&A. As, with questions of one, many can learn.
Cadila, Sanofi,Zydus, AstraZeneca,Mylan,Interview Questions with Sharma Ji,ASK Mechnology,emainfo,Qualistery - GMP Content,easy medical device