February 6-8, 2018Anaheim Convention CenterAnaheim, CA
2018 Event Content Schedule
Use the scheduling tool below to browse all the available sessions, speakers and topics at this year's event. Find the content and sessions to fit all of your educational needs and ensure you get the most out of your time at the show.
MD&M: Product Development Best Practices
Clinical data from registries can be a source of inspiration for alternate uses of a device or line extensions. Leveraging relevant clinical data may lead to more devices being granted marketing authorization, which will increase the availability of medical devices with appropriate labeling to support safe and effective device use in patients. This approach can potentially streamline the process for establishing an intended use claim, and enhance and encourage device development programs. In this session, you’ll hear from an expert on how it’s done.
Topics to be covered include:
Driving new product demand with PMAs
Building your safety profile with registry data
Uncovering new ideas clinicians and patients may have for devices or line extensions