For continuous safety and quality!
The market launch of a medical device is only the beginning. With effective post-market surveillance (PMS), you can monitor the performance and safety of your products in real-world use. Our experts develop customized PMS strategies that integrate seamlessly into your risk management system and comply with current regulatory requirements.
Our PMS services include the following:
- Data analysis and evaluation: We collect user feedback, clinical data, and safety reports.
- For us, risk management means the early detection of potential risks and the proactive implementation of optimization measures.
- We prepare PMS reports in accordance with MDR and other international standards.
- Continuous improvement by adapting your products and processes based on real-world events.
We are the experts in post-market surveillance. With our help, you can ensure the safety, quality, and performance of your medical devices even after they have been placed on the market – and in a sustainable manner.