LAB INFORMATICS
Zylon QA/QC LIMS
Zylon QA/QC LIMS is designed for routine and process-critical quality laboratories that need controlled sample identity, specification-led testing, traceable observations, technical review, quality approval and dependable reporting in one laboratory information lifecycle.
Capability model
Built around controlled laboratory work.
Sample registration & staging
Capture source, batch, product, material, priority, condition, custody and acceptance context before testing begins.
Specifications & test plans
Assign approved tests, methods, limits, instruments, analysts, due dates and responsibility based on sample or product context.
Observation & result capture
Record observations, calculations, units, instrument references and result evidence within controlled laboratory workflows.
OOS, OOT & exceptions
Route rechecks, investigations, deviations and other exceptions without losing the original analytical record.
Technical review & approval
Separate execution, review and approval where required and retain attributable decision history around released results.
Reports, dashboards & trends
Generate controlled laboratory reports and monitor TAT, workload, exceptions, approvals and quality trends.
Controlled process
From laboratory action to traceable evidence.
State-driven workflows, role-based responsibility and reviewable activity help preserve the context behind scientific and quality decisions.
Register
Create the governed laboratory sample and identify its quality context.
Plan
Apply specifications, methods, tests, instruments and responsibilities.
Execute
Capture observations, calculations and analytical results.
Review
Evaluate exceptions, evidence and technical acceptability.
Approve & release
Authorise the result and issue the controlled laboratory output.
Enterprise readiness
Designed to operate as part of the enterprise.
QA/QC LIMS can exchange governed context with ERP, manufacturing, quality, identity, instrument, finance and reporting systems. Typical interfaces may include materials, batches, specifications, sample requests, users, results and release status.
Governed access
Organisation, site, role and responsibility context can govern access to critical records.
Configurable workflows
Approval paths, states, escalations and exceptions can follow the laboratory operating model.
Integration ready
APIs and controlled interfaces can connect ERP, identity, instruments, portals and surrounding systems.
Validation conscious
Implementation can support requirements, verification, controlled change and validation evidence where applicable.