3X Faster Processing. Higher Accuracy. 40% More Business Value. Global Regulatory Monitoring and Intelligence Platform for MDR Compliance

Medical-device manufacturers must transition legacy products from the EU Medical Device Directive to the more stringent Medical Device Regulation. This flyer presents a global regulatory monitoring and intelligence platform developed with Microsoft technologies and powered by specialized AI copilots and intelligent agents. The cloud-native solution uses prebuilt knowledge connectors, an agentic AI framework, and continuous compliance capabilities to accelerate document processing, improve accuracy, and reduce operating cost. It helps quality and regulatory teams manage evidence, documentation, timelines, and compliance workflows more efficiently.