Medical Devices 2020 - 7 secrets about Understanding the Design Verification and Validation Requirements for Medical Devices Training Online

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.
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 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.