Flinn.ai develops purpose-built software solutions to automate quality and regulatory compliance processes for medical device manufacturers. Trusted by over 100 MedTech leaders, Flinn’s validated platform streamlines post-market surveillance (PMS) activities, including global safety database monitoring, literature evaluation, regulatory change tracking, and complaint management.
With AI-powered features like smart intake forms, IMDRF automation, and impact analysis, Flinn helps teams reduce manual work and accelerate decision-making, while ensuring compliance with leading standards such as IEC 62304, ISO 14971, ISO 27001, and FDA 21 CFR Part 11. The platform integrates seamlessly with existing systems, delivering actionable insights while saving time and costs for compliance teams.
