Migrating from a Homegrown or Generic CMS to Matrix eIFU

A smooth, validated migration path away from homegrown or generic CMS solutions that were never built for medical device regulatory requirements.

The challenge
Our solution

How Matrix eIFU makes migration easy

A guided path away from unvalidated, hard-to-maintain systems.

Structured, supported migrationA dedicated migration process with onboarding support at every step.

  • Structured migration process with dedicated onboarding support

  • Data transfer and bulk import of existing IFU documents and metadata

  • UDI mapping and linking carried over from your existing system

Zero disruption cutoverKeep existing labelling working while you migrate.

  • URL redirect support to maintain existing device labelling

  • Parallel running period to ensure zero disruption

  • Validation documentation to support your QMS change control

Removes the IT burdenNo internal IT resource required to maintain the platform.

  • No IT resource requirements — maintained by Matrix eIFU

  • Reduces growing compliance risk of non-validated systems

  • Frees your team to focus on business-relevant work

Hear from our customers

Moving from paper to electronic IFU with Matrix eIFU was perfectly guided and supported. No more printing, shipping, or inventory of paper IFUs — and a significant financial benefit for our organisation.

Regulatory Affairs Manager, Leading orthopedic devices manufacturer in Switzerland

Matrix One is trusted by 500+ Life Sciences & Medical Device Companies