Pharmaceuticals

ISO/IEC 17025 Readiness Achieved in 6 Months

A pharmaceutical laboratory standardized its calibration workflow and reached audit readiness with liquid bath and dry block systems aligned to ISO/IEC 17025 expectations.

The laboratory needed a more defensible calibration workflow for regulated product release and internal quality systems. Indeecon supported the lab with stable reference equipment, better documentation discipline, and a clearer calibration path.

Challenge

The client had fragmented calibration practices across temperature-sensitive instruments and struggled to maintain consistency between operators, records, and reference points.

Solution

Indeecon deployed a combination of liquid bath and dry block calibration equipment, helped define a repeatable SOP structure, and aligned the setup to the lab’s ISO/IEC 17025 documentation needs.

Outcomes

  • Audit readiness achieved within 6 months
  • Better repeatability across internal calibration runs
  • Reduced manual reconciliation effort in documentation
  • Improved confidence in release-critical temperature records