Corrective and Preventive Action Procedure | ISO 13485 | FDA QSR Compliant

SKU: SOP 8-004
$149.00
$149.00
Unavailable
per item
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 Procedure

The Corrective and Preventive Action (CAPA) procedure governs the process to initiate, investigate, implement and track corrective and preventive actions.

Corrective and Preventive Action - Overview

The 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 - Compliance

The 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

RELATED LINKS

​Nonconforming Material Procedure
Failure Investigation Procedure
Medical Device Quality Management System BASE PLUS
​​Medical Device Quality Management System MANUFACTURING
​Medical Device Quality Management System MANUFACTURING PLUS
ISO 13485 Corrective and Preventive Action Procedure
ISO 13485 CAPA Procedure

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