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.
For taking a demo with our team.
The challenge
Homegrown and generic CMS solutions were not built for this
- Not validated for GxPGeneric systems lack the audit trail, version control, and UDI linking that regulators expect.
- Hard to scaleAs portfolios grow, homegrown solutions become harder to maintain and more error-prone.
- IT burden keeps growingInternal maintenance, and retaining the people who built it, becomes a growing cost and risk.
Our solution
A structured, supported migration to a validated platform
- No IT resource requiredOff-the-shelf software maintained entirely by Matrix eIFU.
- Guided migrationA structured process with dedicated onboarding support.
- Zero disruptionA parallel running period ensures continuity of market availability throughout.
How Matrix eIFU makes migration easy
A guided path away from unvalidated, hard-to-maintain systems.
Structured, supported migration
A 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 cutover
Keep 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 burden
No 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
