Ensuring Consistency And Accuracy Of Equipment: Outsourcing To ISO 17025 Accredited Suppliers

By Dustin Williams, ISO 17025 Consultant, Tech Engines

Accurate and consistent measurement results are critical for pharmaceutical manufacturing, where even minor discrepancies can lead to nonconformances. Equipment such as pipettes, analytical balances, and spectrophotometers must be precisely calibrated to ensure reliability. One of the most effective ways to mitigate risks in pharmaceutical equipment calibration is by outsourcing to an ISO 17025 accredited laboratory.

ISO 17025 accreditation signifies that a lab has undergone rigorous third-party audits to verify compliance with quality and technical standards. These accredited labs maintain a robust quality management system (QMS), conduct proficiency testing, and adhere to strict procedures for measurement uncertainty, calibration intervals, and conformity assessments. Pharmaceutical companies benefit from working with ISO 17025 accredited suppliers by ensuring their calibration needs meet industry standards, minimizing operational risks, and maintaining regulatory compliance.

When selecting a calibration provider, companies should verify the lab’s accreditation certificate and scope of accreditation. This ensures the lab has been evaluated for the specific measurements and equipment required. Accredited laboratories are subject to annual audits, maintaining their compliance with ISO 17025 standards and reinforcing trust in their calibration processes.

Outsourcing to an accredited lab is not just a best practice but a strategic decision that safeguards product integrity and regulatory adherence. By prioritizing ISO 17025 accreditation, pharmaceutical companies enhance accuracy, reliability, and compliance in their operations. Ensuring calibration is handled by accredited experts reduces risks and supports long-term success in a highly regulated industry.