Achieve ISO 17025 Faster: Modernize your Laboratory
In this webinar, we examine how compliance performs in real laboratory environments, where audit friction originates, and what structurally audit-ready operations look like in practice.
Video Overview
Laboratories rarely struggle with ISO/IEC 17025 because they lack documentation. They struggle when operational blind spots surface under audit pressure.
When evidence must be reconstructed, traceability breaks across systems, or critical decisions depend on individual memory, audits become disruptive — findings repeat, timelines extend, and operational confidence erodes.In this webinar, we examine how ISO/IEC 17025 performs in real laboratory environments and why accreditation alone does not guarantee operational control.
We explore where audit friction originates, how fragmentation accumulates over time, and what structurally audit-ready operations look like in practice.
What you will learn in this webinar:
- Where operational blind spots typically appear in accredited laboratories
- What auditors actually assess — beyond documentation volume
- Why fragmented processes increase audit pressure and repeat findings
- How digitization reduces audit friction by enforcing control at the moment of execution
- How myLIMS enables system-based compliance, end-to-end traceability, and defensible results
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