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CAPA Management

A seven-stage corrective and preventive action workspace.

Each CAPA is a case workspace with a stable number and a lifecycle: Requested, Investigation (RCA and containment), Action plan (corrective and preventive items with approval), Implementation, Verification, Effectiveness, and Closed. A failed effectiveness check returns the CAPA to the action plan.

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Capabilities

What you can do

Root cause analysis

Findings, RCA method, root cause, and containment in Investigation.

CAR & PAR items

Corrective and preventive line items with plan approval.

Effectiveness check

Pass closes; Fail loops back—no paper CAPA that closes on hope.

Many sources

Link inspection findings, instruments, competencies, and quality studies.

Connected features

Works hand in hand with

Inspection Rounds

Checklists for CLIA, CAP, and internal audits—with linked evidence.

Checklist rounds
Linked evidence
Findings to CAPA

Client Services

Specimen Incidents

Receipt, discrepancy, grossing, and histology problems—tracked to resolution.

Guided wizard
Typed incidents
Status workflow

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