
At Cuviva, we prioritize patient safety, data security, and regulatory compliance. Our RPM Platform is proudly CE-marked as a Class IIa medical device under MDR, covering not just the platform but also all dashboards and features. This certification ensures that we meet the highest European standards for medical devices.
We maintain continuous monitoring of our platform’s safety, performance, and regulatory compliance. Every update and new integration undergoes rigorous testing before implementation, guaranteeing quality and transparency throughout the product lifecycle.
Protecting sensitive health data is at the core of our mission. Cuviva employs advanced encryption, strict access controls, and near-real-time monitoring to safeguard patient information. Regular security audits and a robust incident response plan ensure compliance with the latest healthcare data protection standards.
Want to learn more about our compliance framework and data security?
Feel free to contact us here.