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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.

Matrix eIFU
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