Flinn is an AI-driven platform that automates regulatory and quality processes for MedTech manufacturers. Their unique approach leverages AI to enhance efficiency and ensure compliance with MDR and IVDR regulations. This transformation allows clients to focus on strategic tasks while maintaining regulatory adherence.
Automate post-market surveillance reporting for medical devices; Streamline literature reviews for regulatory compliance; Monitor safety databases for real-time updates; Generate audit-ready reports with one click; Enhance complaint handling processes for efficiency.
Trusted by over 100 MedTech leaders; Complies with IEC 62304 and ISO/TR 80002-2 standards; Achieved 99% uptime with ISO 27001 certification.