Post Market Surveillance for Medical Devices and IVDs
ePMS

ePMS - Your Comprehensive Solution for Post Market Surveillance

Streamline Your MDR PMS and IVDR PMS Compliance with Our Automated Software

‍In the rapidly evolving medical device and IVD industry, staying compliant with Post Market Surveillance (PMS) regulations is paramount. At meddevo, we understand the complexities of MDR PMS and IVDR PMS compliance. That's why we've developed ePMS, a comprehensive Post Market Surveillance software designed to simplify your compliance process.

Automated and Synced Post Market Surveillance

Our ePMS software offers an automated and synced solution for Post Market Surveillance. It allows you to plan your activities, generate evidence, and keep your documentation up-to-date. With ePMS, you can automate the creation and update of PMSP, PMSR, PSUR, and many more, ensuring you never miss a revision.

eTD - Single Source of Truth

Based on the meddevo eTD standard ePMS serves as a single source of truth for your technical documentation. With shared content and no redundancy, ePMS keeps your technical documentation clean and organized. It also ensures that you never forget to revise your documents, saving you time and reducing the risk of non-compliance.

Collaboration and Process Automation

Our software solution promotes collaboration and process automation, making it easier for your team to work together and stay on the same page. With ePMS, you can streamline your Post Market Surveillance process, improve efficiency, and ensure that your medical devices and IVDs meet the highest standards of safety and performance.

Experience the Future of Post Market Surveillance

Ready to experience the future of Post Market Surveillance? Learn more about ePMS and discover how our software can streamline your MDR PMS and IVDR PMS compliance.

Want to learn more about automation of regulatory processes and technical documentation? Join the University!