At DeSia, we support you in developing effective post-market strategies for your medical devices / in vitro diagnostic medical devices, ensuring ongoing compliance and patient safety.
What We Offer
- Preparation of tailored PMCF and PMPF plans/reports based on your device’s clinical or clinical performance data
- Coordination and management of follow-up activities in collaboration with your team
- Documentation and analysis of real-world data to monitor safety and performance
- Integration of findings into your existing clinical or performance evaluation processes
Our services help ensure your device continues to meet regulatory expectations throughout its lifecycle.
Do you need support with your post-market follow-up activities? Book your complimentary initial consultation.