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 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.
"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."