Achieve and Maintain Compliance
With MDR and IVDR
Ensure that data on the quality, performance, and safety of devices are gathered, recorded, and analyzed
Introducing
Post-Market Intelligence
Post-Market Clinical Follow-up
Systematic Literature Review
Post-Market Surveillance
At A Glance
Quality
Performance
Safety
How We Help
Systematic Literature Review

There is not enough talent to review the volume and velocity of medical literature that must be analyzed. Empowering existing talent is the best goal.
Post-Market Clinical Follow-up

Data bottlenecks need to be removed and processes need to be optimized to make reporting on clinical performance more effective and efficent.
Post-Market Surveillance

Pro-active and systematic data must be collected for conclusions about preventative and corrective actions. Some products have far too much data to review, some far too little.
Watch this 1-minute video to more about the benefits of Huma.AI's validated Machine Learning solution for meeting the post-market challenges of EU MDR and IVDR.