The Medical Devices Conference on Tools, Technologies, and Strategies to Accelerate Your Time to Market is dedicated to regulatory updates and guidance to speed up the time to market in the medical device industry and smooth the transition to 3rd Edition of IEC 62304, IEC 60601, obtaining CE Mark and Pre-Market Approval etc.
Designing software and managing risks in an FDA regulated medical environment and improving human-to-device interfaces.
Confirmed/pending speakers include representatives from the CSA International, FDA, the Underwriter Laboratories and TUV.
