{"id":4959,"date":"2026-09-01T10:50:21","date_gmt":"2026-09-01T13:50:21","guid":{"rendered":"https:\/\/gboetrack.com\/?p=4959"},"modified":"2026-09-01T10:51:50","modified_gmt":"2026-09-01T13:51:50","slug":"auditoria-laboratorial-sua-pre-analitica-esta-pronta-todos-os-dias-ou-apenas-na-semana-da-visita","status":"publish","type":"post","link":"https:\/\/gboetrack.com\/en\/auditoria-laboratorial-sua-pre-analitica-esta-pronta-todos-os-dias-ou-apenas-na-semana-da-visita\/","title":{"rendered":"Laboratory audit: Is your pre-analytical process ready every day, or only during the week of the visit?"},"content":{"rendered":"

Anyone who manages diagnostic medicine operations knows the drill well: as soon as the accreditation audit date approaches, teams go into high alert. The race begins to check physical files, fill in gaps in contingency spreadsheets, and hope that no non-conformities have gone unnoticed at the sample collection stage.<\/p>\n\n\n\n

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This pre-audit stress reveals a classic symptom: when quality control relies on manual or paper processes, compliance becomes a temporary effort, not an operational habit.<\/p>\n\n\n\n

The truth is straightforward: a laboratory of excellence should not need to \u201cprepare\u201d for an audit. The process needs to be auditable by definition, at every moment.<\/p>\n\n\n\n

The end of paper-based evidence<\/strong><\/p>\n\n\n\n

In the pre-analytical phase\u2014where up to 70% of diagnostic errors occur\u2014demonstrating compliance has always been a bottleneck. How can one demonstrate to an auditor, with mathematical precision, that tourniquet time limits were observed, that sample homogenization followed protocol, or that the sample's chain of custody remained intact from the bedside to the centrifuge?<\/p>\n\n\n\n

With eTrack<\/a>, Greiner Bio-One\u2019s aim has always been to turn compliance into an automatic byproduct of work well done:<\/p>\n\n\n\n