Focus on safety and performance
The launch of a medical device marks the beginning of a continuous process. Effective post-market clinical follow-up (PMCF) ensures long-term success by enabling ongoing monitoring of clinical performance.
Through the systematic collection and analysis of real-world application data, we identify potential risks, validate benefits, and continuously optimize your products – always in accordance with the latest regulatory requirements.
Our offering includes the following PMCF services:
- Individual PMCF plans are developed as part of the project work.
- Conducting observational studies and surveys
- Detailed data analysis and risk assessment.
- Preparation of regulatory PMCF reports
- Continuous optimization of risk management
We offer you our expertise to comprehensively monitor and improve the safety and performance of your medical devices even after they have been placed on the market.