Cold storage rooms

Cold storage validation and monitoring for pharmaceutical facilities

Complete visibility across multiple cold rooms and sites. Standardized processes and audit-ready documentation for FDA, EMA, and more.

The problem

No visibility across sites

Most organizations rely on manual checks, fragmented systems, and multiple vendors for cold room compliance. Legacy systems lack redundancy, and a single overnight failure can destroy product before anyone notices. Tracking multiple rooms across sites with different processes creates compliance risk. When auditors ask for documentation, teams hunt through spreadsheets instead of producing reports in seconds.

The solution

Unified compliance across all locations

Eupry monitors temperature and humidity continuously, alerting the right staff via SMS, email, and call when conditions drift. Generate audit-ready reports in 3 clicks, combining validation, monitoring, and calibration data with automatic traceability across all sites in one platform. ISO-accredited calibration happens on-the-wall in seconds. Built-in redundancy ensures no single point of failure. Compliant with FDA, EMA, and more.

DSV Sweden

“Eupry was very professional and informative throughout the process, providing us with high-quality service (...) It's undoubtedly a well-put partnership.”

Joakim Sund

Quality Assurance Specialist

Eagle Air Freight

“Eupry was instrumental in helping us establish a GDP-compliant operation ready for the standards of pharmaceutical logistics. Their flexibility, expertise, and collaborative approach were exactly what we needed to navigate the requirements of the industry and develop a foundation that worked for us."

Mike from Eagle Air Freight

Michael O'Brien

President

Download our Product Catalog

Get an overview of how Eupry’s products can help with automatic monitoring and mapping of temperatures, humidity, CO2 and diff. pressure.

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