In regulated environments – pharmacies, laboratories, hospitals, or research facilities – compliance with standards is not just a goal: it’s a legal requirement and a condition for operating. This means continuously and rigorously monitoring environmental conditions like temperature, humidity, pressure, or air quality.
But managing this manually is a heavy, high-risk task: spreadsheets to fill out, readings to compile, incidents to log… A single oversight or undetected deviation can lead to non-compliance, the loss of critical products, or even penalties or accreditation withdrawal.
That’s where automated monitoring systems like those from ATEK turn these constraints into simple, reliable… and auditable processes.
Being compliant is not just about “taking the temperature” once a day. You need to be able to prove at any time that you monitored, reacted, corrected, and documented – flawlessly – over several years.
Regulatory authorities typically require:
Every manual step increases the risk of human error. And every error or omission is a risk – for your products, your patients… and your compliance.
ATEK’s automated environmental monitoring solutions meet these regulatory demands while turning a burden into a strategic advantage.
Certified, high-precision sensors measure and record critical parameters (temperature, humidity, CO₂, differential pressure, etc.) continuously.
No data is lost, all measurements are timestamped and stored automatically – a major asset in audits or surprise inspections.
As soon as a threshold is breached (e.g., refrigerated products above 8°C), an alert is instantly sent to the right people by SMS, email, or push notification.
This enables immediate intervention – even during nights or holidays.
Every action (adjustments, transfers, maintenance) can be logged in just a few clicks directly within the ATEK platform – complete with supporting evidence.
No more forgotten notes or last-minute justifications: full traceability is ensured.
Reports are automatically generated – with history, graphs, annotations, and digital signatures.
Auditors don’t need to search through binders: everything is clear, accessible, and compliant with GxP, FDA 21 CFR Part 11, ISO 17025, Health Canada, BNQ, and more.
This ease of access and validation accelerates your audits and streamlines the process of obtaining or renewing certifications.
All data is stored in a highly secure cloud environment, with redundancy, encryption, and protection from tampering.
Your historical records remain available for years – and meet the long-term retention requirements of regulatory bodies.
We support our clients beyond the technology itself:
Audits and inspections shouldn’t be a source of stress.
With ATEK, you’re always ready, with zero effort.
Our experts are ready to assess your needs, design a custom solution, and train your team.
👉 Contact us today to turn regulatory compliance into a strategic asset.