Medical Devices 2021 - Understanding the Design Verification and Validation Requirements for Medical Devices Webinar

Design Verification and Validation (DVV) for Medical Devices is getting a lot of attention today as it is very challenging to understand and fulfil the DVV needs for Class I to Class III devices. In the current environment of global standardization of quality and regulatory
To understand and fulfill the ever growing, complex Design Verification and Validation (DVV) requirements to manufacture, register and launch your medical device in a timely manner.
Will review FDA DVV definitions and expectations based on her personal experience in executing DVV in device companies
Will incorporate several examples based on the FDA 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.