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On-demand webinar

Overcoming calibration challenges in GxP

Calibration deadlines slipping? Vendors out of sync? Certificate overload?

Calibration can be a labor-heavy and risk-filled process. Join us for a session where we explore the main challenges of calibration in GxP and the practical steps to overcome them.

  • Certificate overload and missing data

    Calibration certificates pile up, and auditors often find gaps: missing uncertainty values, no reviews of certificates, or incomplete traceability.

  • Unclear sensor calibration intervals

    Annual calibration is not always the answer. Regulators expect risk- and reliability-based intervals – something most QA teams lack the time and tools to prove.

  • Out-of-tolerance (OOT) management

    When devices drift, auditors often ask how the impact was assessed, and teams can lack a clear process for this and corrective actions.

  • Multi-site process inconsistency

    Different sites and vendors often follow different calibration practices, leading to gaps, higher costs, and inconsistent audit outcomes.

Calibration is a common compliance headache in GMP and GDP

QA teams must keep track of device status, ensure timely calibration, manage vendors, document and store certificates, and retrieve records buried in a million different systems (and filing cabinets).

At the same time, inspectors raise questions about calibration types, chosen points, uncertainty, traceability, and accreditation – questions that are often complex and resource-heavy to answer.

The result? Calibration drains time, creates compliance risks, and remains a frequent source of audit findings.

In this webinar, we explore the core calibration challenges in GxP environments and share practical strategies to overcome them.

Key takeaways

  • 5 components your calibration process should include in GxP
  • Which calibration records inspectors always expect to see
  • Accredited vs. traceable calibration (and when to choose each)
  • How to set and defend calibration intervals for GDP and GMP
  • How to handle out-of-tolerance findings without failing an inspection

About the speakers

  • Anja Lundin Jacobsen: QA/QC Lead at Eupry, expert in biomedical laboratory science and daily operations in Eupry’s ISO17025-accredited calibration lab.
  • Jakob Konradsen: Co-founder and Chief of Quality at Eupry, electrical engineering background with extensive experience in validation, monitoring, and calibration.