Medical Devices Conference ™ Tools, Technologies and Strategies to Accelerate Your Time to Market Any lag in getting products to market is costly on every front from cash expenditures to loss of market share and the evaporation of the first-to-market competitive edge. Designing medical devices that meet the complex safety certification and regulatory requirements are the most common reasons for delays, especially if these requirements are not known in the early stages of design. With the transition to the 3rd Edition of IEC 60601 globally, the approval process is expected to be more challenging and time consuming than ever. Are you ready for the transition? Do you understand the new requirements?

Fortunately the lag can be shortened substantially with a better understanding before the design phase, to include proper regulatory guidance and the use of a pre-submission evaluation process. These measures can increase product safety and prevent costly errors and delays from accidental omission of vital information. 

Groundbreaking program highlights includes:

An exclusive 90-minute Q&A with the FDA, Underwriter Laboratories, and TÜV Critical updates regarding the 3rd Edition of IEC 60601, pre-market approval (PMA), auditing psrocess, documents requirement, and any other questions you have! 20+ leaders and expert sessions on the latest and most critical discussion on regulatory compliance, software design and development, improving usability, and much more.

The Medical Devices Conference will put you in front of regulatory and Notified Bodies’ officials and experts who will provide you with such guidance to speed your time to market and smooth the transition to IEC 60601.  There are also workshops and podium presentations in key issues from improving human-to-device interfaces to designing software and managing risks in an FDA regulated medical environment. 

With so much at stake, can you really afford to operate without this information?  Join us  at the Medical Devices Conference and get up to speed now!