Corrective and Preventive Action Procedure | ISO 13485 | FDA QSR Compliant
SKU:
SOP 8-004
$149.00
$149.00
The ISO 13485 Corrective and Preventive Action (CAPA) procedure governs the process to initiate, investigate, implement and track corrective and preventive actions.
- ISO 13485:2016 Compliant
- FDA QSR Compliant
- Includes Related Forms
- MS Word Format
- Digital Content - Instant Download
Corrective and Preventive Action ProcedureThe Corrective and Preventive Action (CAPA) procedure governs the process to initiate, investigate, implement and track corrective and preventive actions.
ISO 13485 Corrective and Preventive Action OverviewThe Corrective and Preventive Action (CAPA) procedure provides a means for coordinating action plans resulting from information obtained from several sources. The Corrective and Preventive Action (CAPA) Procedure includes instruction and all supporting forms, for CAPA initiation, CAPA Plan and CAPA Plan Closure.
Corrective and Preventive Action Procedure ComplianceThe Corrective and Preventive Action Procedure is FDA QSR and ISO 13485:2016 compliant.
To learn more about our Corrective and Preventive Action (CAPA) Procedure contact us at info@aplyon.com
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ISO 13485 CAPA Procedure
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