Five temperature tiers, continuously monitored, fully recorded.
Storage is not shelf space. It is a monitored range, a documented chain of custody, a plan for what happens when the power fails, and a record you can hand an auditor two years from now.
+15 → +25 °C
Controlled room temperature
Ambient-stable materials held inside a defined, monitored range — not simply left in the room.
- Lyophilised reagents
- Plasticware and consumables
- Kit components
- Buffers and media
+2 → +8 °C
Refrigerated
The working temperature of most of the life-science world, and the tier where excursions cost the most.
- Antibodies and enzymes
- Sera and cell culture media
- IVD reagents
- Biologics and vaccines
−20 °C
Frozen
Standard frozen storage for nucleic acids, controls and aliquoted material.
- Nucleic acids and plasmids
- Aliquoted serum
- Assay controls
- Temperature-sensitive enzymes
−80 °C
Ultra-low
Deep frozen storage and dry-ice transport for material that cannot see a warm minute.
- mRNA and viral vectors
- PBMCs and tissue
- Long-term biospecimens
- Master and working banks
≤ −150 °C
Cryogenic
Liquid nitrogen vapour phase, in dry shippers that hold their charge across an international lane.
- Cell and gene therapy material
- Stem cells
- Cryopreserved PBMC
- Reproductive tissue
Monitoring and excursion handling
Continuous electronic temperature monitoring with alarming, not a clipboard and a daily walk-past. When a reading leaves range, the excursion is recorded, you are notified, and the material is quarantined pending your disposition decision — because the call on whether product is still fit for use is yours to make, not ours.
- Continuous electronic monitoring with alarm thresholds per tier
- Documented excursion procedure — record, notify, quarantine, await disposition
- Time-out-of-range captured and reported, not summarised away
- Mean kinetic temperature reporting where your protocol calls for it
- Physical checks on a fixed schedule in addition to electronic monitoring
Inventory that speaks your language
- Receipt against your paperwork, with discrepancies raised before put-away
- Lot and expiry captured at receipt
- FEFO and FIFO rotation
- Quarantine, on-hold and released stock held separately
- Sample-level retrieval, not just pallet-level
- Cycle counting
- Documented destruction and disposition
What we will not claim
We do not describe our facility as cGMP, validated, temperature-mapped or GDP-certified, because those words mean completed qualification work with documentary evidence behind them. When that work is done we will publish the evidence. Until then you get a plain description of what is installed and how it is run — ask us and we will walk you through it, or come and look.
Tell us what you need to move, and at what temperature.
Send us the materials, the temperatures and the destinations. We will come back with a scope and a price — not a discovery call.