In this presentation, DQS will present some insights into post market surveillance for medical device manufactures, addressing the requirements of different jurisdictions and the value of PMS as a tool for business assurance and sustainable growth. Using case studies, we will explore the application of various PMS strategies, evaluating the pros and cons to enable you to apply this knowledge to your own medical devices.
Learning Objectives:
Be aware of the differences in PMS requirements in the US and EU/UK
Understand how PMS design can contribute to business assurance
Be aware of different approaches to PMS and how to apply them to different devices