This Corrective and Preventive Action Procedure complies with ISO 13485:2016, EU MDR 2017/745, and FDA QMSR 21 CFR 820. Delivered in editable Word format, it defines processes for identifying, investigating, correcting, and preventing quality issues. Digital delivery within 24 business hours.
This procedure ensures systematic handling of non‑conformities and potential risks by implementing corrective and preventive actions. It covers root cause analysis, corrective measures, preventive planning, and effectiveness verification. Delivered in editable Word format for customization. Consultancy services are available via email, Zoom, or on‑site visits. Full implementation or signed, approved procedures are offered at an extra fee.