Get a comprehensive overview of your device statuses and performance metrics in one place.
Generate detailed reports and stay on top of your compliance requirements effortlessly.
Maintain accurate records and efficiently manage device data for better decision-making.
Receive timely alerts for maintenance, performance, and compliance actions.
PMS Copilot streamlines MDR 2017/745 compliance with cost-efficient automation of Post-Market Surveillance (PMS) tasks, including PSUR generation. Our solution reduces compliance costs, accelerates reporting, and helps medical device companies focus on delivering safer, high-quality products to market.
We provide tools that help automate compliance workflows, reduce administrative burden, and ensure that your medical devices meet regulatory requirements. With real-time dashboards and audit trails, you'll always have the visibility you need to maintain compliance standards.
We help you stay compliant with all relevant medical device regulations, ensuring your equipment is always ready for inspection.
Schedule and manage regular maintenance tasks to keep your medical devices functioning optimally.
Our experts provide training and support to ensure your team can make the most of our device management system.
We provide tools that help automate compliance workflows, reduce administrative burden, and ensure that your medical devices meet regulatory requirements. With real-time dashboards and audit trails, you'll always have the visibility you need to maintain compliance standards.
Our platform provides end-to-end management of the medical device lifecycle, from acquisition to retirement. Stay informed about device health, usage history, and maintenance requirements to make informed decisions and optimize your equipment's performance.
"PMS Copilot has revolutionized the way we handle our medical equipment. It makes compliance and management so much easier."
"We love how intuitive and user-friendly this platform is. It has saved us a lot of time and effort in managing our devices."