Enhance your QMS – Corrective Action/Preventive Action
Corrective Action/Preventive Action, the CAPA system
The CAPA system is a mechanism that identifies and implements any changes necessary to ensure and maintain
the continued effectiveness of the Medical Device Manufacturers (MDM) Quality Management System (QMS).
Does your company need help in CAPA remediation and aligning with ISO 13485 and 21 CFR Part 820.100 requirements? Contact Network Partners.