Continuous monitoring for pharmaceutical cleanrooms
You need continuous evidence that differential pressure, temperature, humidity, and CO₂ stay within limits between qualification cycles, with records that hold up under audit.
Classification is a snapshot. Audits are continuous.
Cleanroom classification confirms a room can meet its grade. Annex 1 and FDA inspectors look for evidence the room did meet its grade across every shift, every batch, every excursion. Most facilities run separate systems for differential pressure, temperature, humidity, and viable monitoring – which means manual reconciliation, documentation gaps, and partial-parameter coverage when the URS calls for more.
One platform across every cleanroom parameter
Eupry covers differential pressure, temperature, humidity, and CO₂ in one GxP-compliant system. Continuous data, real-time alerts the moment conditions drift, and audit-ready records under 21 CFR Part 11 and EU GMP Annex 11. Calibration happens on-the-wall in minutes. One vendor, one system, every parameter your contamination control strategy requires.
“All of the loggers have proven their worth and saved precious samples on several occasions when freezers broke or were accidentally left open.“
Anja Pomowski
Senior Scientist Antibody Production at Antikor
“I would absolutely recommend Eupry to other companies. I’m saving a lot of time (...) There is no travel involved and I can do the data collection and reporting remotely. Eupry’s program is the only one that I’ve found that can do that. This applies well to the US.”
Daniel Wassell
Equipment Validation Engineer
“It took me under an hour to calibrate 40 loggers – including the time it took to find the refrigerators.”
Kasper H. Christophersen
Research Associate at Novozymes
Relevant products
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Get an overview of how Eupry’s products can help with automatic monitoring and mapping of temperatures, humidity, CO₂, and differential pressure.
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