Remediation Services for Medical Devices

Publish date:

Changing medical regulations around documentation needs, mergers and acquisitions, and product upgrades are leading to an increasing need for product remediation support services in the medical device industry. Companies need to ensure faster time to market of the product and be compliant to the demanding regulatory scrutiny. Capgemini with its industrialized approach to product remediation […]

Changing medical regulations around documentation needs, mergers and acquisitions, and product upgrades are leading to an increasing need for product remediation support services in the medical device industry. Companies need to ensure faster time to market of the product and be compliant to the demanding regulatory scrutiny.

Capgemini with its industrialized approach to product remediation can support clients at an optimized cost and in a scalable, consistent, and transparent manner. Our trusted approach is built on key pillars of expertise in medical devices, system engineering, electro-mechanical disciplines, and specialization in regulatory affairs and quality management services.

Related Resources

Digital Engineering and Manufacturing Service

Compliance with the new EU MDR and IVDR

Medical and in-vitro diagnostic device manufacturers must meet strict deadlines over the next...

Digital Engineering and Manufacturing Service

Solutions for Medical Devices Digital Technical Publications

The implementation of the new Medical Device Regulation (MDR), the In-Vitro Diagnostic...

Digital Engineering and Manufacturing Service

Solutions for Medical Devices and Healthcare

Capgemini’s medical device engineering practice brings solutions and services that help our...