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Cadena de frío for the laboratory

An area that brings together all of the laboratory's temperature-controlled storage equipment: biomedical refrigerators (+2 to +8 °C), freezers (-20 to -40 °C) and ultra-low temperature freezers (-80 °C), designed to keep samples, reagents, drugs and blood components stable, with the uniformity, alarms and recording that a domestic appliance cannot offer.

cadena de frío guide

Storage of vaccines, medicines and reagents; blood banks and blood components; biobanks and sample collections; plasma and biologicals; enzymes and strains; and regulated storage in hospitals, pharmacies, clinical laboratories, the pharmaceutical industry and research.

How to choose cadena de frío

  • It depends on the temperature the material requires (+2 to +8 °C refrigeration, -20/-40 °C freezing, -80 °C ultra-low)
  • The volume and interior organization
  • The alarms and recording required by the applicable regulation
  • The backup available in the event of a power failure
  • And the energy cost of continuous operation. Specific values come from the catalog (Sanity)

Frequently asked questions about cadena de frío

What temperature does each type of material need?

As a reference: +2 to +8 °C for vaccines, drugs and reagents in routine use (biomedical refrigerator); -20 to -40 °C for plasma, enzymes and biologicals (freezer); -70/-80 °C for critical long-term biological material such as nucleic acids, cells and biobanks (ultra-low temperature freezer). The material defines the equipment, not the other way around.

Why not use domestic appliances in the laboratory?

Because they guarantee neither uniformity nor stability: they have cold and warm spots, recover slowly after the door is opened, and lack alarms and recording for auditing. Biomedical-grade equipment keeps the temperature homogeneous, alarms on deviations, and documents storage conditions.

How do I protect the cold chain against power failures?

With equipment that has good thermal retention, local and remote alarms (audible, remote or to the cloud), continuous temperature recording and, for critical loads, electrical or CO₂/LN2 backup, all within a documented contingency plan.

What is required to qualify this equipment in a regulated environment?

Installation and operational qualification (IQ/OQ) plus thermal mapping with load and calibrated sensors, and recording compliant with 21 CFR Part 11 where applicable. Inolab, together with Meling and Binder, installs, qualifies and services the entire cold chain in Mexico.

Brands we represent in cadena de frío

Available cadena de frío models

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