Corrective and Preventive Action Log

CAPA template

Corrective and Preventive Action Log for medical device CAPA management

Use this editable Corrective and Preventive Action Log to record nonconformities, root causes, corrective and preventive actions, and verify their effectiveness.

Structure CAPA workflowsMove from detection to root cause, action and effectiveness.
Link to audits and complaintsConnect CAPA inputs to audit findings and post-market feedback.
Demonstrate ISO 13485 complianceProvide objective evidence of effective corrective action.

  • Best for: CAPA processes, nonconformity management, root-cause analysis and effectiveness checks.
  • Includes: editable sections for problem description, root cause, action plan and effectiveness verification.
  • Format: editable template available through the standard WooCommerce download flow.
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Lexqara helps manufacturers build CAPA systems that close quality gaps and satisfy notified-body expectations. Explore the Resource Center or review our Quality Management System Audit Services.

Description:
This CAPA Log template gives us a single, controlled view of every CAPA so we can track progress, owners, deadlines, and closure decisions without losing evidence.

  • Register each CAPA using a unique CAPAYYYY-XXX identifier.

  • Capture source of issue (audit, complaint, PMS, supplier, NC product) for traceability.

  • Record status across the CAPA phases (from initiation to closure).

  • Assign responsible owner/pilot and due dates for each milestone.

  • Link root-cause analysis outputs to the action plan.

  • Track effectiveness evaluation evidence and acceptance criteria.

  • Record Quality Manager review and final approval/signature at closure.

Your needs:

  • CAPA log template

  • CAPA log template for ISO 13485 and MDR compliance

  • Reduce rework, control timelines, and improve audit readiness.

Use this log whenever a CAPA is opened, updated, or closed so we maintain an up-to-date management overview of corrective and preventive actions within our QMS.

It focuses on accountability. CAPA is the controlled process to correct issues and prevent recurrence. Effectiveness evaluation confirms actions worked against measurable criteria.

  • Maintain an up-to-date CAPA status overview.

  • Track owners, due dates, and overdue actions.

  • Record root-cause completion and linked evidence.

  • Document action implementation and supporting records.

  • Capture effectiveness outcomes and conclusions.

  • Confirm documented closure approval and archiving.

At Lexqara, we help implement CAPA workflows that connect audits, complaints, PMS signals, and risk management—supported by training and inspection-ready records. Visit our Resource Center [https://lexqara.com/resource-center] and Audit & Inspection Support [https://lexqara.com/services/audit-and-inspection-support]. ISO 13485 overview [https://www.iso.org/standard/59752.html]. Download the template or request a short gap assessment.

A well-run CAPA log improves visibility, strengthens management review inputs, and reduces repeat findings by keeping actions measurable and traceable.

Template preview

Template preview: Corrective and Preventive Action Log

Review the key sections included in the Corrective and Preventive Action Log template before downloading it. This preview shows the structure and content you will receive in the editable file.

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Sheet: LOG-CAPA

CAPA Log LOG-CAPA-001
CAPA # Initiation Date Origin Short Description Pilot Devices involved Priority HHE Status Date of Root-Cause Analysis Date for Action Plan Closure Date for Effectiveness Check Date of Closure Priority Status
CAPA2024-00X YYYYMMDD NCYYYY-001 HHEYYYY-XXX YYYYMMDD YYYYMMDD YYYYMMDD YYYYMMDD Critical Evaluation
Major Investigation
Minor Root-cause Analysis
Non-Significant Action Plan Definition
Action Plan Implementation
Verification of Effectiveness
Closed

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