Cambio CIS achieves MDR Class IIb certification

Cambio CIS has achieved MDR Class IIb certification, one of the highest levels of regulatory scrutiny for medical device software under the European Medical Device Regulation (MDR).

The certification confirms that Cambio CIS meets the stringent requirements for patient safety, product quality, risk management and regulatory compliance set out in the MDR.

For customers, it provides added assurance that Cambio CIS continues to be developed, maintained and supported to the standards required for software used in critical clinical environments – strengthening confidence in the product and securing a compliant foundation throughout its lifecycle.

Visit the product page or contact Jon Dahlen for more information.