Simplify post market surveillance (PMS)
Six steps to effective post market surveillance under MDR and IVDR
Post market surveillance is more than a regulatory requirement. It is a continuous process for gathering, analyzing and acting on real-world data to ensure the ongoing safety and performance of medical devices and in vitro diagnostic medical devices.
In this guide, you'll learn:
- The 6 key steps in an effective PMS process
- How PMS, PMCF/PMPF, CAPA and risk management connect
- PMS Report and PSUR requirements by device class
- How to turn post-market data into meaningful actions
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