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

$149.00
$149.00
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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
SKU: SOP 8-004

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 [email protected]

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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