Quality Assurance and Regulatory Affairs for Medical Devices (QARA)

Publish date:

Solutions for Medical Devices

With the rapid changes taking place in medical technologies the regulations and quality requirements also need to keep pace and address the specific needs across different geographies. For Medical Devices, the regulatory compliance requirements kick in and play a crucial role from the product design phase and provide guidelines across the product lifecycle.

Capgemini helps organizations to adhere to the stringent norms under the product regulations to stay relevant in the market.


File size: 328.64 KB File type: PDF


File size: 1.13 MB File type: PDF

Related Resources


Securing Enterprise IoT from Vulnerabilities and Breaches

Intel and Capgemini have combined their security expertise to deliver an end-to-end IoT...


Keep your employees safe with Pega

Ensure the wellbeing of your workforce while mitigating business risks


AI In Healthcare

A comprehensive approach to drive Business Value through AI, Intelligent Automation &...