How to generate Real-World Data through Post Market Surveys
Real‑World Data (RWD) has become a major focus across the MedTech industry, driven by evolving regulatory expectations and the increasing emphasis on Real‑World Evidence (RWE). Recent regulatory developments, including FDA guidance on the use of RWE and proposed changes to simplify EU MDR and IVDR, have important implications for how RWD is generated and assessed for medical devices.
Post Market Surveys, including Post‑Market Clinical Follow‑up (PMCF) and Post‑Market Performance Follow‑up (PMPF) surveys, provide manufacturers with a structured way to generate real‑world data on device safety and performance once products are on the market. Used effectively, these approaches can support regulatory and commercial requirements across different stages of the device lifecycle.
Download this complimentary infographic to explore:
How PMCF, PMPF and other survey methodologies are used to generate RWD
When surveys are most appropriate across the device lifecycle
Key considerations for real‑world data collection and regulatory use
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