LabZila ISO 17025 LIMS software helps testing and calibration laboratories manage methods, personnel competency, equipment, calibration, samples, quality-control activities and audit records in one connected system. Maintain clearer traceability, organize assessment evidence and support consistent laboratory operations across your accreditation scope.
ISO/IEC 17025 establishes requirements for the competence, impartiality and consistent operation of testing and calibration laboratories. Accreditation bodies assess both management and technical requirements against the standard.
Manage the technical and quality records needed to support consistent laboratory operations and ISO/IEC 17025 accreditation activities.
Create, review, approve and maintain methods, SOPs and quality documents with controlled version histories.
Maintain complete, searchable records for samples, testing, calculations, observations, results and approvals.
Track laboratory equipment, calibration schedules, maintenance activities, status and supporting certificates.
Plan audits, document findings, assign follow-up actions and monitor progress through closure.
Record nonconforming work, assess impact and track corrective actions, responsibilities and effectiveness reviews.
Manage qualifications, training, competency assessments and method-specific personnel authorizations.
Control approved methods, specifications, acceptance criteria, validation evidence and review dates.
Connect samples, methods, analysts, equipment, reference standards and results throughout the testing process.
Schedule management reviews and document inputs, decisions, responsibilities and improvement actions.
Maintain user-attributed, time-stamped and traceable laboratory records across connected workflows.
Connect technical activities, quality records and accreditation evidence through one traceable laboratory workflow.
Define the accreditation scope, approved methods, personnel, equipment and quality requirements.
Complete testing or calibration using authorised personnel, suitable equipment and controlled methods.
Verify technical records, calculations, QC results, traceability and reportable data.
Conduct internal audits, record nonconforming work and identify actions requiring follow-up.
Manage corrective actions, effectiveness checks, management-review decisions and process improvements.
Keep methods, competency, equipment, audits and supporting records current for accreditation assessments.
Centralize technical and quality records to support consistent laboratory operations and accreditation readiness.
LabZila supports configurable ISO 17025 workflows across laboratories managing methods, competency, equipment, quality records and assessment evidence.
ISO/IEC 17025 is the international standard that defines requirements for the competence, impartiality and consistent operation of testing and calibration laboratories. It helps laboratories demonstrate that they are technically capable of producing valid and reliable testing or calibration results.
LabZila helps laboratories organize methods, personnel competency, equipment, calibration, samples, QC results, audits and corrective-action records in one connected LIMS. These capabilities can support accreditation preparation and ongoing record management, but accreditation is granted by an accreditation body after assessing the laboratory’s management system and technical competence.
Yes. LabZila can centralize equipment profiles, calibration schedules, maintenance histories, current status, reference standards and supporting certificates. Equipment records can also be connected with methods, samples and test results to provide clearer technical traceability.
LabZila maintains controlled access, user-attributed activities, time-stamped record histories, connected source records and review workflows. These controls help laboratories maintain complete and traceable information, while data integrity also depends on approved procedures, training, suitable system configuration and responsible user practices.
Yes. Laboratories can schedule internal audits, define their scope, record findings, assign responsible users and monitor follow-up actions through closure. LabZila also helps organize related documents, evidence and corrective actions so records are easier to retrieve during assessments.
Yes. LabZila can record nonconforming work, document impact assessments, assign corrective actions, set due dates and track review and effectiveness activities. Formal corrective-action and CAPA workflows can be connected with audits, complaints, methods, equipment, samples and other affected laboratory records.
LabZila can be configured around the users, methods, equipment and workflows required by a smaller laboratory and expanded as operations grow. The appropriate setup depends on the laboratory’s accreditation scope, sample volume, data-migration needs, integrations and quality processes.
LabZila can connect with compatible laboratory instruments and external systems through supported interfaces, APIs or structured data formats. The integration approach depends on the instrument model, available communication method, data output and the laboratory workflow that needs to be supported.
Strengthen Accreditation-Supporting Workflows
See how LabZila can help your testing or calibration laboratory manage methods, competency, equipment, quality records and assessment evidence in one connected LIMS.