3Aware

At 3Aware, we’re passionate about transforming the MedTech landscape through our innovative platform, aiSurveillance™. Our solution is a first-of-its-kind software specifically designed for the real-time surveillance of medical devices throughout their post-market life cycle. We understand that global medical device manufacturers are faced with increasingly complex post-market regulatory requirements. The new EU Medical Device Regulation (EU MDR) necessitates extensive real-world data collection for post-market clinical follow-ups (PMCF), a task that has traditionally required significant time and resources.

That’s why we’ve developed our unique platform that combines three essential solutions into one: Access, Analysis, and Alerts. This comprehensive approach allows MedTech companies to efficiently gather and analyze real-world patient health data, ensuring that their products remain safe and effective for users. By leveraging AI and real-world evidence, we empower clinical and regulatory teams to make informed decisions swiftly, enabling them to maintain their market presence while optimizing costs. Our mission is clear: to alleviate the burdens of data collection and enhance product safety, thus improving the healthcare experience for everyone.