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2025-09-02 13:39:08 -

Digitalizing CAPA Workflows to Strengthen Post-Market Surveillance and Complaint Handling

The Rising Urgency of CAPA Transformation in the Medical Device Sector The medical device industry operates under constant regulatory scrutiny, where safety, efficacy, and compliance are non-negotiable. As post-market surveillance intensifies across regions like the US, Europe, and Asia-Pacific, manufacturers are compelled to address quality challenges with agility and precision. Issues...

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