PMS Copilot is a software platform that simplifies post-market surveillance and compliance management for medical devices. It centralizes device data, automates compliance workflows, and generates reports to help organizations stay audit-ready. The platform also provides maintenance scheduling and training support to streamline daily device management.
Funding
Funding not disclosed
Founders
Product
Problem
Medical device manufacturers and healthcare organizations often struggle to manage post-market surveillance (PMS) activities, including device tracking, compliance documentation, and performance monitoring. Manual processes are time-consuming, error-prone, and can lead to regulatory gaps during audits.
Solution
PMS Copilot provides an intuitive platform that centralizes medical device management and automates post-market surveillance workflows. The solution helps organizations track devices, maintain accurate records, and generate compliance reports with minimal manual effort. It also delivers automated alerts for maintenance, performance, and compliance actions, ensuring that critical tasks are not missed. Built-in training and support resources help teams maximize the platform's value and maintain regulatory readiness.
Target Audience
Primary users are medical device manufacturers, healthcare facilities, and regulatory affairs teams that need to manage post-market surveillance and maintain compliance with medical device regulations.
Features
- Device reporting tools that generate detailed compliance reports and streamline regulatory documentation
- Centralized data management for maintaining accurate device records and supporting informed decision-making
- Automated alerts and notifications for maintenance schedules, performance monitoring, and compliance deadlines
- Maintenance scheduling capabilities to keep equipment in optimal condition and inspection-ready
- Expert-led training and support to help teams effectively use the system and stay compliant