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Humidity & Temperature Calibration for CAP & CLIA Clinical Laboratories

Femto Scientific provides ISO/IEC 17025 accredited humidity and temperature calibration that keeps clinical and diagnostic laboratories CAP- and CLIA-ready — NIST-traceable certificates with as-found and as-left data and documented uncertainty for the humidity probes, sensors, and data loggers guarding your reagent and specimen storage, refrigerators, incubators, and controlled-environment monitoring systems.

  • Calibrated to ensure accuracy for survey
  • NIST-traceable RH reference standards
  • As-found & as-left data on every certificate
  • Documented measurement uncertainty (k=2)
  • Survey- and inspection-ready documentation
  • Onsite service for high-volume labs
  • Reagent & specimen storage monitoring calibration
  • Automatic recertification scheduling

Humidity and temperature records your CAP inspector can check off without a second question.

Humidity Calibration Requirements for CAP and CLIA Laboratories

Clinical laboratories accredited by the College of American Pathologists (CAP) or operating under CLIA must calibrate the environmental monitoring instruments that control storage conditions with NIST-traceable standards and keep the records available for survey. ISO/IEC 17025 accredited calibration is the cleanest way to demonstrate that competency for every reagent refrigerator, specimen freezer, incubator, and controlled-environment monitor.

CAP Survey Readiness (LAP)

CAP accreditation program (LAP) checklists require documented calibration of environmental monitoring instruments with NIST-traceable reference standards and established calibration intervals. Our certificates document NIST-traceable calibration, the calibration date, as-found/as-left results, and reported uncertainty — exactly what surveyors expect in a CAP survey binder.

CLIA 42 CFR 493.1252

CLIA requires instruments to be maintained and calibrated per manufacturer and quality-standard specifications, using NIST-traceable references within the established interval. Our accredited humidity and temperature certificates meet those requirements and integrate directly with your LIMS and inspection documentation.

Reagent & Specimen Storage Environments

An out-of-tolerance humidity sensor can compromise reagent, control, and specimen storage or a temperature-critical assay. Accredited calibration with documented uncertainty and as-found data gives you the evidence to demonstrate storage validity — and to scope any impact if an environmental monitoring sensor is found out of tolerance.

Humidity sensor and data logger calibration for a CAP/CLIA clinical laboratory

A Full Calibration, Not Just a Single-Point Spot Check

An in-house spot check confirms a single point; it is not a calibration. Accredited calibration characterizes performance across your use range with NIST-traceable references and documents it for CAP and CLIA compliance. Both belong in your quality program — serving different purposes.

  • Multi-point RH calibration across the clinical range
  • Humidity probes, sensors & combination probes
  • Data loggers & environmental monitoring sensors
  • As-found & as-left data with adjustment
  • Documented expanded uncertainty (k=2)
  • Electronic certificates for paperless QMS

Most CAP and CLIA laboratories calibrate environmental monitoring equipment at least annually. Compare service levels and turnaround on the humidity & temperature calibration service page, or add continuous ARTEMIS remote temperature & humidity monitoring for your reagent and specimen storage.

CAP & CLIA Humidity Calibration FAQs

Keep Every Clinical Humidity Sensor Survey-Ready

Send us your instrument count and types — we’ll return a quote with turnaround options and a recommended calibration interval that keeps your laboratory inside CAP and CLIA requirements year-round.

Request a CAP/CLIA Quote +1-800-631-0263