Flinn helps MedTech manufacturers stay compliant while boosting efficiency with AI-powered solutions for post-market surveillance (PMS) processes.
Flinn is an AI-driven platform to automate your regulatory and quality processes, ensuring full compliance with MDR and IVDR. It supports MedTech companies in handling low to high-risk medical devices and managing portfolios of any size, from SMEs to enterprises with thousands of technical files.
- Automate global safety database monitoring
- AI-assisted literature evaluation and regulatory monitoring
- Streamline complaint handling and post-market surveillance reporting
- Generate audit-ready reports with one click