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
ech transfer brings new equipment, new mapping studies, and other new qualification work.
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
Tech transfer is a near-constant event at a working CDMO.
Continuous Mapping and Monitoring (CMM) replaces periodic re-mapping with always-on data – the same loggers monitoring the room generate the mapping evidence.
- No re-mapping studies disrupting suites twice a year
- Faster equipment qualification for new client onboarding
- Mapping evidence available the moment an auditor asks
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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 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 the info you need to assess our compliance.
Digital quality as a commercial asset
Sponsors grade CDMOs on digital quality maturity during supplier qualification. With Eupry, you have the auditable, real-time compliance infrastructure pharma expect.
- 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
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Talk to our team, or get the full platform overview in the product catalog.