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Curoflow’s platform is a CE-registered medical device in accordance with the EU Medical Device Regulation (MDR) (EU) 2017/745.
All data within the platform is encrypted, stored, and processed in compliance with the EU’s General Data Protection Regulation (GDPR). Our proprietary video solution also ensures that all data is handled exclusively in Europe—without relying on third-party tools from the US, where GDPR compliance cannot be guaranteed.
This sets Curoflow apart from most other solutions on the market, which typically rely on providers like Microsoft, Zendesk, Zoom, Twilio, and AWS.
If you want full confidence that all your data is handled and stored in full compliance with GDPR, Curoflow is the clear and simple choice.
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Curoflow is CE-marked according to the EU Medical Device Regulation (MDR) and is under the supervision of the Swedish Medical Products Agency. All development is conducted in accordance with MDR and its associated quality management system.
This certification demonstrates our strong commitment to data security and privacy within healthcare.
We would be happy to discuss your business and how Curoflow’s various features could make it more efficient. Send us a message and we will book a demo of the platform and tell you more!
Email: contact@curoflow.com
Telephone: +46 (0)10 – 750 06 55
