Article September 2, 2026 · 8 min read

LabCollector · AgileBio

Introducing Enterprise QC and Calibration Management in LabCollector LIMS – LSM v4.2

We are pleased to announce LSM v4.2, introducing a new Enterprise Quality Control and Calibration workbench for LabCollector LIMS. This release connects QC plans, calibration runs, laboratory instruments, analytical batches and customer results within a single controlled workflow — replacing disconnected spreadsheets and manual checks with a traceable, integrated quality process.

From QC Planning to Customer Results

Laboratories can now create version-controlled QC plans defining:

  • Standards, blanks, controls and replicates
  • Required instruments and reference materials
  • Run sequences and recurring checkpoints
  • Acceptance criteria and calculation rules
  • Validity periods and usage limits
  • Review, approval and activation requirements

Approved plans remain available while future revisions are drafted. When a replacement is approved, the previous version is retired without compromising historical runs.

QC Plans module in Lab Service Manager — version-controlled plans with draft and approved statuses
QC Plans — version-controlled plans with draft and approved statuses, side by side.

Controlled QC and Calibration Runs

The new QC Run Workspace guides analysts through execution:

  • Generate fresh internal QC jobs and samples
  • Enter or import results using standard LSM workflows
  • Record materials, lots and certificate values
  • Review each reference as Pass or Fail
  • Reanalyse failed references without losing previous evidence
  • Exclude unsuitable references with authorization and justification
  • Calculate governed outputs
  • Submit runs for review, approval and activation

Every important action is recorded in the audit trail.

QC Run Workspace — ordered run sheet with calibration outputs and audit timeline
QC Run Workspace — the ordered run sheet, live calibration outputs and audit timeline in one view.

Calibration Outputs in Customer Calculations

Approved QC outputs can be used directly in customer-result formulas through controlled variables such as:

{QC:XRF_FE_FACTOR}

LSM resolves each variable from the QC run assigned to the relevant batch, assay and instrument. Supported calculations include:

  • Recovery
  • Correction factors
  • Mean and standard deviation
  • Slope and intercept
  • Minimum and maximum
  • Sequence-specific correction factors

Raw numerical precision is retained for calculations, while normal parameter settings control displayed rounding.

Results management — raw signals and calibrated concentrations governed by the assigned QC run
Customer results — raw signals and calibrated concentrations governed by the assigned QC run.

Reference-Level Acceptance

Plans can require an explicit Pass or Fail decision for each calibration reference. They can also define the minimum number of accepted references needed to calculate a factor — only accepted references contribute to governed averages.

A failed reference must be resolved by either:

  • Creating a fresh, traceable reanalysis; or
  • Recording a justified exclusion by an authorized user

This provides flexibility without weakening traceability.

Batch-Level QC Governance

LSM v4.2 introduces strong links between analytical batches and QC runs. Before customer results can progress, LSM verifies:

  • Required QC coverage
  • Instrument compatibility
  • Run validity
  • Available capacity
  • Checkpoint status
  • Factor availability
  • Assignment consistency

A single assay can be governed by separate QC runs for different instruments. Associations remain attached to the customer executions as permanent evidence. When a run no longer has sufficient capacity, LSM blocks the affected work and guides users toward preparing another run or splitting the remaining samples into a new batch.

Reusable Calibration and Batch Correction

Two operating models are supported:

  • Reusable calibration — one approved run can serve multiple compatible batches until its validity or capacity is exhausted.
  • Batch correction — the QC run and its factors are permanently associated with one analytical batch.

Correction factors can follow strategies such as:

  • Last accepted reference
  • Mean of accepted references to date
  • Final accepted run mean

This supports workflows where a reference measured after a defined number of customer samples becomes effective for the following sequence.

Quality Review and Impact Management

Authorized reviewers can inspect:

  • Run configuration and execution
  • Source observations
  • Reference decisions
  • Material and certificate evidence
  • Calculated outputs
  • Acceptance rules
  • Checkpoints
  • Audit history
QC Runs list — runs with IN_PROGRESS, DRAFT, ACTIVE and SUPERSEDED statuses
QC Runs — the full list with IN_PROGRESS, DRAFT, ACTIVE and SUPERSEDED statuses, including next checkpoints and remaining usage.

If an active QC run later fails or becomes unsuitable, LSM can identify potentially affected customer results and support documented impact assessment.

Built for Controlled Laboratory Environments

The new workbench includes:

  • Granular permissions
  • Separation of duties
  • Mandatory reasons for controlled actions
  • Immutable source-result snapshots
  • Optimistic locking and transactional updates
  • Audited QA overrides
  • Multilingual interfaces
  • A built-in HTML user manual
  • Demonstration data for evaluation and training

Available in LSM v4.2

Enterprise QC and Calibration Management is available as an optional feature in LSM v4.2 for LabCollector LIMS. It brings calibration evidence, analytical execution and customer reporting together — helping laboratories replace disconnected spreadsheets and manual checks with a traceable, integrated quality workflow.

Ready to see it in action? Visit LabCollector to learn more about LSM v4.2 and how the new QC & Calibration workbench can strengthen your laboratory's quality process.

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