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.
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.
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.
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.
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.
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