Post Market Clinical Follow Up
PMCF is an active collection of data on the clinical experience of your device aftermarket release. PMCF activities can range from an analysis of data from literature or existing device registries to performing a new post-market clinical investigation.
PMCF refers to activities that help provide data, documentation, and evidence regarding a medical device’s safety or performance. PMCF is one component of post-market surveillance (PMS) activities for medical devices.