Autoclave validation services
From qualification to continuous compliance
Eupry offers pharmaceutical autoclave validation without the multi-vendor chaos, long timelines, or surprise costs. Get your steam sterilizers qualified and operational with full IQ/OQ/PQ coverage, digital protocols, and seamless transition to cycle monitoring.
Trusted by 500+ pharmaceutical and biotech companies, including:
The autoclave validation challenge
Long timelines, operational disruption, disconnected compliance
Validation blocks production
Validation providers often have long lead times, and traditional autoclave validation requires weeks of equipment downtime. This creates scheduling nightmares and months of potential production lost.
Requalification restarts the cycle
Every year (or after equipment changes), the whole process starts over: schedule the vendor, block production time, run the same tests, pay the same costs, and get another paper report.
Validation data disconnected from operation
Spend thousands on validation, get a paper binder. Then every cycle requires manual printout review and logbook entries. When auditors ask about performance trends since validation, you are digging through boxes of disconnected records.
Download a product catalog
Get an easy overview of all Eupry’s products from validation to calibration and automated monitoring temperatures, humidity, CO2 and more.
Talk to a specialist
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