Industry · Medical Devices
MES for medical devices plants.
ISO 13485-friendly traceability. Every operator action, every quality hold, every batch — captured in a validated cloud environment.
What medical devices plants tell us
The problems that come up every discovery call.
- Paper DHR records slow audit prep
- Operator authentication weak or missing at machines
- Genealogy across assemblies is guess-and-check
What Xentr deploys
The modules that light up on day one.
- Audit trail
- Genealogy
- Operator auth
- Electronic DHR export
Audit prep time
-70%
Typical outcome in a 90-day rollout. Actual numbers depend on baseline maturity.