FDA Regulated Industries 2021 - Dealing with CAPA- Corrective and Preventive Actions in FDA Regulated Industries Live Webinar

CAPA ( Correcive and Preventive Actions) for FDA regulated arena such as Medical Device, Food and Pharmaceutical industries is getting a lot of attention today by FDA and ISO auditors. CAPA requirements have been tightened for ISO 13485: 2016 requirements
Learn how to interpret FDA and ISO 13485:2016 CAPA requirements for your product to fulfill global pharma and medical device requirements and specifically in the FDA quality and regulatory arena where the different CAPA phases from CAPA problem statement
Will review FDA CAPA definitions and expectations based on her personal experience in closing several CAPAs in FDA regulated industries
Will incorporate several examples based on the FDA CAPA Requirements so you can integrate them into your product risk management for commercialization
Speaker:
Meena Chettiar, has worked as a Scientist for Health Canada and as a Quality Management Professional in food, pharmaceutical and medical device industries for over 25 Years in Canada and the United States.