3Aware aiSurveillance enables access to longitudinal patient level data, including conditions, treatments, encounters, procedures and outcomes, directly related to the use of specifically identified medical devices.
3Aware puts the power to attain clinical outcomes, easily perform scientific analysis and control business spend, back in your hands.
Tens of Millions of Patients, Tens of Thousands of Devices, and Growing
AI-derived Clinical Notes and Interpretation
Platform Optimized for Evolving Compliance, Market Access and Label Expansion Needs
3Aaware enables MedTech manufacturers to achieve compliance at a fraction of the time, cost and risk of status quo approaches, by enabling highly-efficient access to longitudinal patient-level data; including conditions, treatments, encounters, procedures and outcomes–directly related to the use of specifically identified medical devices.
We didn’t retrofit an existing solution for MedTech–every component of 3Aware aiSurveillance was thoughtfully built by MedTech veterans, for MedTech manufacturers–to help you meet our industry’s requirements today, and overcome the challenges of tomorrow.
3Aware aiSurveillance enables high-level aggregated previews of data sources to quickly and easily assess and verify that the required content is present.
3Aware aiSurveillance enables massive populations of patients to be quickly and easily studied and sorted, to identify optimal cohorts for desired results.
3Aware aiSurveillance enables the “gold” buried in unstructured procedure notes to be quickly and easily recognized, interpreted, structured and curated for optimal use.
3Aware aiSurveillance enables the pertinent content to be quickly and easily located and interpreted to most efficiently achieve PMCF compliance objectives, through a combination of our platform, scientific partnership and epidemiological services.
3Aware aiSurveillance enables MedTech Manufacturers and CROs to minimize the time, cost and risk of PMCF.
"*" indicates required fields