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.
Your company shouldn’t be paralyzed by over-analyzing data in determining risk. The amount of time and effort you spend determining risk should be commensurate with the risk and complexity of the device, and this should also hold true during the verification and validation process. In this session, you’ll learn how to right-size your risk assessment efforts and focus on what counts.
Topics to be covered include:
How your company can simplify the risk assessment process to make it more defensible during a regulatory or quality audit
Best practices for using your company’s culture to apply this process
Examining the ties-ins with ISO 13485, ISO 14971, and the new EU Medical Device Regulations
Best practices for simplifying your risk-based approach to product development