Dashboard & sample staging
Prioritise received samples, acceptance checks, containers, custody, assignment and readiness before laboratory execution.
ZYLON SUITE · ENTERPRISE QUALITY CONTROL LIMS
Govern every QC sample, result, review and release decision.
Zylon QC LIMS is the laboratory informatics core for quality-control teams that require secure access, controlled execution, traceable evidence and accountable release decisions. It connects sample receipt, staging, test planning, observations, rechecking, technical review, approval, reporting and quality oversight in one governed environment.
- Protect data integrity from sample receipt to controlled report release
- Separate execution, review and approval responsibilities
- Standardise quality-control processes across laboratories and methods
- Provide traceable evidence for management review, audit and validation
PRODUCT PROOF
Zylon QC LIMS, in operation.
These views use the actual Zylon QC LIMS operating capture. The full workspace is shown first, followed by focused details from the same captured interface and the actual governed Zylon Suite access layer.
The complete captured QC LIMS operating screen connects sample identity, controlled analytical results, status and review responsibility in one laboratory workspace.
A focused view of the same actual capture highlights the dense laboratory result area used to review values, limits and testing context.
This crop keeps the underlying screenshot unchanged while bringing workflow state and accountable review controls into clearer view.
The actual Suite launcher shows how users enter authorised Zylon applications through a common enterprise access layer.
Process controls
Purpose-built control for the work that matters.
Each capability is organised around accountable workflows, governed data, explicit responsibilities and management visibility rather than isolated form entry.
Work orders & controlled test plans
Assign specifications, approved methods, instruments, analysts, due dates and responsibility-aware workflow steps.
Observation sheets & raw data
Capture observations, calculations, units, limits and instrument context in a traceable laboratory record.
Review, recheck & approval
Support rechecking, technical review, quality approval, segregation of duties and attributable decision evidence.
Reports, quality events & complaints
Generate controlled reports and connect deviations, complaints and follow-up activity to the exact samples, tests and approvals involved.
Analytics, auditability & MIS
Monitor TAT, workload, OOS/OOT patterns, rework, approvals and laboratory trends while preserving reviewable activity history.
Controlled workflow
From action to evidence to authorised decision.
Receive & stage
Identify, inspect, accept and prioritise samples under controlled custody.
Plan
Create work orders and allocate approved tests, methods, instruments and responsibilities.
Execute
Capture authorised observations, calculations and instrument-supported results.
Review & approve
Recheck, technically review and complete segregated approval with attributable evidence.
Release & retain
Issue the controlled report and retain the laboratory evidence required for oversight and review.
Shared enterprise governance
Every Zylon application inherits the same control principles.
Security and compliance are applied through identity, responsibility, workflow and evidence so governance does not disappear when a process crosses modules or sites.
Role-based control
Apply organisation, site, role and responsibility context to records and workflow actions.
Process governance
Use controlled states, approvals, escalations and segregated responsibilities for critical decisions.
Traceable evidence
Maintain attributable activity and change history around important records, reviews and approvals.
Validation-conscious design
Support requirements, verification, controlled change and customer validation evidence appropriate to intended use.
Operational outcomes
Convert governed operational data into dependable performance.
Defensible results
Preserve the identity, evidence, context and approval history behind every reported value.
Consistent quality execution
Apply common methods, specifications and governance while supporting authorised local laboratory configuration.
Faster controlled turnaround
Expose queues, due dates, exceptions and review bottlenecks before commitments are affected.
Audit and management readiness
Use traceable records, dashboards and MIS to support investigations, reviews and laboratory performance decisions.