Blog
Articles, guides and industry insights on laboratory digitalization, accreditation and the LIMS world.
ISO/IEC 17020:2026 Published: What Changes for Inspection Bodies
The new edition withdrew the 2012 version on 27 March 2026. Risk-based thinking, the Type A simplification and the 2029 transition deadline.
Read MoreElectronic Signatures in Laboratory Reports: Law and Practice
Qualified certificates, time stamps and ISO 17025 report approval: where electronic signatures sit in the laboratory workflow.
Read MoreData Integrity for QA Teams: ALCOA++ and Audit Trail Guide
The ten principles of data integrity, audit trail requirements and the findings most often raised in laboratories.
Read MoreQuality Management Systems in Laboratories: A Complete Guide
ISO 17025 clause 8 requirements, the ten QMS components, CAPA, internal audits and the move to a digital QMS.
Read MoreLaboratory Audit Processes and TÜRKAK Accreditation
The application process, surveillance assessments, the most frequently raised findings and practical preparation advice.
Read MoreWhat is LIMS? Laboratory Information Management System Guide
What is LIMS (Laboratory Information Management System), why is it needed, and what are its core features? Discover laboratory information management systems with our comprehensive guide.
Read MoreWhy is LIMS Essential for ISO 17025 Accreditation?
Why is LIMS software indispensable for meeting ISO/IEC 17025 accreditation requirements? Everything about traceability, data integrity and accreditation compliance.
Read MoreLaboratory Digitalization Guide
Steps to digitalize your laboratory, ROI calculation and critical points to consider. A step-by-step digital transformation guide.
Read MoreCalibration Certificate Management
Transitioning from manual calibration certificate processes to digital management. QR code verification, e-signature and accreditation-compliant certificate generation.
Read MoreReady to Digitalize Your Laboratory?
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