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Laboratory Calibration Services for Clinical CAP & CLIA Laboratories

Femto Scientific keeps clinical laboratories survey-ready with one ISO/IEC 17025 accredited calibration program across the measuring and support equipment your testing depends on — centrifuges, pipettes, thermometers, temperature-controlled storage, and balances. NIST-traceable certificates with as-found/as-left data give your CAP checklist and CLIA quality records exactly the evidence a surveyor expects.

  • CAP checklist & CLIA quality-system aligned records
  • As-found & as-left data on every instrument
  • Centrifuge, pipette & temperature coverage
  • One accredited program for the whole lab
  • NIST-traceable references for every instrument
  • Documented measurement uncertainty
  • Onsite service to minimize instrument downtime
  • Electronic certificates for your QMS / LIS

Accredited calibration records your CAP surveyor can check off without a second question.

Why CAP & CLIA Laboratories Require ISO 17025 Accredited Calibration

In a clinical laboratory, a centrifuge running off-speed, a pipette out of tolerance, or an unmonitored refrigerator can each compromise patient results. CAP checklists and CLIA regulations require the laboratory’s measuring and support equipment to be calibrated and maintained on a defined schedule with documented records — and ISO/IEC 17025 accredited, NIST-traceable calibration is the cleanest way to demonstrate it.

CAP Accreditation & Checklists

CAP checklist requirements call for instruments and equipment — centrifuges, pipettes, thermometers, and temperature-dependent storage — to be calibrated and function-checked per manufacturer and regulatory requirements, with records retained. Our accredited certificates capture the instrument identity, date, as-found and as-left values against limits, and test-equipment traceability a CAP inspector expects to see.

CLIA 42 CFR Part 493

CLIA requires laboratories to maintain and calibrate equipment following manufacturer instructions and to keep the supporting records (42 CFR 493.1252 and 493.1255). NIST-traceable calibration of your centrifuges, pipettes, and temperature devices supports the equipment side of your CLIA quality system and complements the calibration verification your lab performs on its test systems.

Continuous Survey Readiness

Accredited calibration with documented measurement uncertainty and as-found/as-left data, delivered electronically to your QMS or LIS, keeps your equipment records current and immediately retrievable — helping ensure an unannounced CAP or CLIA survey doesn’t find a gap in your calibration documentation.

ISO 17025 accredited calibration program for a CAP and CLIA clinical laboratory

One Accredited Program Across Your Clinical Instruments

Rather than tracking a separate vendor for every instrument type, put the measuring and support equipment behind your clinical testing on a single ISO/IEC 17025 accredited calibration schedule — with consistent documentation and NIST traceability across all of it.

  • Clinical, blood-bank & benchtop centrifuges (RPM, timer, temperature)
  • Single- & multi-channel pipettes (ISO 8655, gravimetric)
  • Thermometers, probes & temperature data loggers
  • Refrigerators, freezers, incubators & water baths
  • Analytical & precision balances
  • As-found & as-left data with documented uncertainty

Start with the instruments your surveyor asks about most — centrifuge calibration, pipette calibration, temperature calibration, thermometer calibration, and spectrophotometer calibration — or see every service on the calibration services hub.

Clinical CAP & CLIA Laboratory Calibration FAQs

Keep Your Clinical Lab Survey-Ready Year-Round

Send us your instrument list and required service level — we’ll return a quote with onsite scheduling and a recommended calibration interval that keeps your equipment records inside CAP and CLIA requirements all year.

Request a Clinical Quote +1-800-631-0263