Eupry provides a GxP-compliant platform that integrates automated temperature and humidity monitoring, mapping, and calibration into a single solution for regulated industries. This system eliminates manual processes, reduces audit preparation time by up to 70%, and ensures continuous compliance with ISO and FDA standards.
Funding
$23.8M raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
CAFounders
Product
Problem
Regulated industries face challenges in maintaining consistent temperature and humidity compliance due to disconnected, manual processes for monitoring, mapping, and calibration. These disjointed systems increase the risk of data loss, audit reporting errors, and potential compliance failures, leading to wasted time and resources.
Solution
Eupry offers a GxP-compliant platform that integrates automated temperature and humidity monitoring, mapping, and calibration into a single, unified solution. This system eliminates manual data collection, reduces audit preparation time, and ensures continuous compliance with ISO and FDA standards. Eupry's wireless data loggers provide real-time monitoring, while its patented sensor tip technology enables rapid calibration without device swapping. The platform consolidates all compliance data, including calibration certificates, temperature records, and audit-ready reports, into a single source of truth.
Target Audience
Eupry's primary customers are companies in regulated industries such as pharmaceuticals, biotech, logistics, and laboratories that require temperature and humidity compliance.
Features
- Wireless data loggers for continuous, real-time temperature and humidity monitoring, even during Wi-Fi outages
- Patented sensor tip technology for fast, on-site calibration without removing data loggers
- ISO 17025-accredited calibration process with digital certificate storage
- Automated mapping solutions with digital reporting and GxP-compliant equipment
- Centralized platform for storing calibration certificates, temperature records, deviation documentation, and audit-ready reports
- Instant deviation alarms and automatic documentation to minimize risks
- FDA 21 CFR Part 11 module for compliance