While the exploding medical device market offers growth opportunities, it demands safety along innovation from the technology providers. Learning key requirements of the FDA 510K clearance process and the newly added “Human Factors” to deliver quality products on time is critical to your success as a developer. Get the updates!
In this intense single-day training event experts will share their expertise and years of experience to help you streamline the FDA process and minimize risks to stay competitive in your product development. You will also learn essential information such as new changes of IEC 60601-1 3rd edition (ES 60601-1), IEC 62304 and ISO 14971 in medical device development designed just for you. As an added bonus, you will gain insight on the medical devices design and validation process (both software and hardware) which will help you get a head start.
Register online at: http://medsmagazine.com/events/