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ISO/IEC 17025 Parameter

Equipment Validation

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Service Overview

Thermal mapping, validation, and qualification (IQ/OQ/PQ) for critical cleanrooms, warehouses, autoclaves, and freeze dryers.

Calibration Process Workflow

1

Placing multi-channel loggers across spatial grids

2

24-to-72 hour temperature logging cycles under load states

3

Compiling hot and cold spot spatial charts

4

Issuing validation report package

Standards Followed

FDA 21 CFR Part 11ISPE GAMP 5WHO Annex 9 (Warehouses)

Applications

  • Pharmaceutical cold warehouse compliance mapping
  • Sterilizer autoclave validation runs
  • Cleanroom air particulate classification audits

Equipment Calibrated

  • Sterilizing Autoclaves
  • Cold Chain Warehouses
  • Stability Testing Chambers
  • Ultra-low Temperature Freezers

Benefits

  • Fully guarantees food and medicine storage criteria
  • Ensures compliance with KSA SFDA audits
  • Verifies absolute temperature uniformity across large spaces

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