Temperature and environmental compliance for CDMOs
A dozen client audits a year on top of regulatory inspections. With Eupry, every record you need is a few clicks away.
- Mapping, monitoring, and calibration in one platform
- Temperature, humidity, CO₂, and differential pressure
- Audit-ready reports in 3 clicks
Trusted by CDMOs and the industry's largest pharma manufacturers
Compliance at a CDMO never stops
Audits, audits, and more audits
Sponsor audits land every one to two years per client, on top of regulatory inspections from the FDA, EMA, MHRA, and others.
Every new client is a new validation
Set points change from client to client. New mapping studies, new documentation, new qualification work – every time.
One facility, many configurations
Different suites, different parameters – temperature, humidity, CO₂, DP – each with its own vendor and system.
One QMS, many sponsor SOPs
Different sponsors, different SOPs, different reporting formats – one shared infrastructure has to satisfy them all.
One platform, every facility, every product, every client
Eupry covers monitoring, validation, and calibration of temperature, humidity, CO₂, and differential pressure on one system.
Every fridge, freezer, incubator, cleanroom, warehouse, and cold room in one place.
Local quality teams work in their own data, central quality gets the full overview.
Continuous mapping for constant tech transfer
When set points change for a new client, your existing mapping data is no longer valid.
Continuous Mapping and Monitoring (CMM) replaces periodic re-mapping with always-on data. The same loggers monitoring the room generate the mapping evidence, ready whenever set points or clients change.
- Digital re-mapping conducted in a few clicks
- New set points, new documentation – without starting from scratch
- Mapping evidence available the moment an auditor asks
Download a product catalog
Prevent mistakes and stop the hunt for data with automated monitoring built for GMP, GDP, and other GxP industries. Get instant access to all the details and see how it works in our catalog.
Audit-ready data integrity, for FDA and every client
Eupry is built on the data integrity regulators and sponsors expect:
- Fully validated software with a specialised 21 CFR Part 11 module
- EudraLex Annex 11 compliant electronic records
- ALCOA+ aligned audit trails on every reading
- ISO 27001-certified data security with AES encryption
- Pre-calibrated loggers with ISO 17025 certificates
- Export-ready reports for FDA, EMA, and sponsor audits
Find all certificates, accreditations, and other info you need to assess our compliance.
Digital quality as a commercial asset
CDMOs compete on capacity, capability, and increasingly on digital quality. Sponsors grade you on all three during supplier qualification.
With Eupry, you have the auditable, real-time compliance infrastructure pharma expects.
- Real-time dashboards your sponsors can be shown directly
- Audit-ready data packages on demand, not assembled by hand
- One validated system across every suite, every site
- Easier sponsor qualification, stronger renewals
Used by 1000+ companies worldwide
Use cases
From cold storage rooms to autoclaves, Eupry's solutions cover environmental compliance for every CDMO use case.
Cold storage rooms
Complete visibility across multiple cold rooms and sites. Standardized processes and audit-ready documentation for FDA, EMA, and more.
Fridges and freezers
24/7 visibility for vaccines, biologics, and temperature-sensitive samples. Instant alerts, built-in redundancy, and audit-ready documentation for FDA, EMA, etc.
Autoclaves
Autoclave validation without the box. Wireless loggers that survive steam sterilization, with real-time monitoring and automated compliance documentation.
Incubators and climate chambers
You run stability studies or cell cultures that require precise and stable temperature and humidity control. You need reliable monitoring that catches problems immediately, not during the next check.
Ultra low freezers (ULTs) and cryos
24/7 visibility for samples stored from -80°C to -196°C. Instant alerts, built-in redundancy, and audit-ready documentation for FDA, EMA, and more.
Warehouses
GDP compliance documentation that impresses clients. Validation that does not disrupt operations. One provider for monitoring, mapping, and calibration.
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Talk to our team, or get the full platform overview in the product catalog.