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Explore IQVIA by region
As a global community, IQVIA continuously invests and commits to advancing human health.
Americas
Europe
Asia & Oceania
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EMEA Thought Leadership
White Paper
Maximizing post-market surveillance with real world data
Medical device recalls are on the rise at the same time as the EU MDR and IVDR are bringing increased post-market surveillance (PMS) requirements.
Apr 18, 2020
- Library
- Maximizing post-market surveillance with real world data
Get instant access
EU Medical Devices Regulation and In Vitro Diagnostics Regulation are bringing increased post-market surveillance (PMS) requirements for all MedTech firms.
Multiple factors, including the rapid growth in device interoperability, the rise in Software as a Medical Device (SaMD), and increasingly frequent cybersecurity breaches, have been responsible, in part, for the continued rise in recalls, particularly software-related recalls. In this Executive Summary of a recent webinar learn about:
- Challenges with post-market surveillance
- Understanding real world evidence
- The future post-market surveillance safety landscape
- How to set up a better post-market surveillance approach