CAPA Issuing & Reviewing

CAPA Issuing & Reviewing

Correct Issues. Prevent Recurrence. Strengthen Compliance.

AGON supports pharmaceutical facilities in managing corrective and preventive actions (CAPA) to sustain compliance and strengthen operational efficiency. We help quality teams accurately identify deviations and non-conformities, implement corrective actions that eliminate root causes, and establish preventive controls that ensure issues do not recur. Our approach ensures that every CAPA is timely, traceable, evidence-based, and aligned with global regulatory expectations for continuous improvement.

What We Deliver

Identification and documentation of deviations, non-conformities, and audit findings
Development of corrective and preventive action (CAPA) plans with defined timelines and ownership
Review and verification of CAPA implementation to ensure effectiveness and closure
Guidance to prevent recurrence and promote CAPA-driven continuous improvement

Deliverables

CAPA reports with detailed corrective and preventive actions, responsibilities, and implementation timelines
Verification and closure documentation for regulatory readiness
Recommendations for process and system improvements to enhance compliance and quality performance

Categories

We understand the importance of approaching each work integrally and believe in the power of simple.

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