CAPA Management

Corrective and preventive actions are improvements to an organisation’s processes taken to eliminate causes of non-conformities or other undesirable situations. The CAPA module assists medical device companies to take control of incidents, deviations and corrective actions. Replacing a paper-based CAPA process with an electronic system and connecting it with change control, training and other quality systems can help assure the problem can never be experienced again.


  • Reduce risk of non-compliance
  • Report and track quality events
  • Trace issue root cause

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