⚠️ Challenges we face in this sector

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    High-precision temperature control (±0.5 °C) to preserve drug efficacy

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    Mandatory backup emergency system with redundant compressors

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    Continuous data logging retained for 5 years for audit compliance

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    GMP, GDP, and WHO PQS certifications

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    Storage of sensitive vaccines at -70 °C for certain types

✅ Our integrated engineering solutions

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    Dual Lead/Lag refrigeration: if one compressor fails, the standby unit starts automatically

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    Data loggers certified to CFR 21 Part 11 standards

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    Thermostats with ±0.1 °C accuracy and yearly calibration

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    -70 °C ultra-low rooms for mRNA vaccine storage

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    Instant SMS, email, and sound alarm notifications

Technical Specs

Optimal Temperatures for Products

Reference table for thermal requirements of each product, used by our engineers in designing precise refrigeration systems

Product Temperature Relative Humidity
General medications +15°م إلى +25°م 60%
Refrigerated medications +2°م إلى +8°م 55%
Conventional vaccines +2°م إلى +8°م —
mRNA vaccines (Pfizer) -70°م —
Blood plasma -30°م —
Tissue and biological samples -80°م —
Past Clients

We executed projects in this sector for top companies

Pharmaceutical distributors across the Eastern Province
Frequently Asked Questions

Customer questions about this sector

Which GMP certification is required for pharmaceutical cold rooms? +
GMP (Good Manufacturing Practice) requires per-minute temperature logging, a backup refrigeration system, instant out-of-range alarms, full maintenance documentation, yearly equipment calibration, and at least 4 hours of stable temperature retention during a power outage.
How are mRNA vaccines kept at -70 °C? +
We use Ultra-Low Temperature Freezers built on a two-stage Cascade system using R404a in the first stage and R23 in the second, with CO2 backup and high redundancy to prevent vaccine loss.

Planning a refrigeration project in this sector?

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