This Management Review Procedure complies with ISO 13485:2016, EU MDR 2017/745, and FDA QMSR 21 CFR 820. Delivered in editable Word format, it defines the process for top management to review the quality management system at planned intervals, ensuring its continuing suitability, adequacy, and effectiveness. Digital delivery within 24 business hours.
This procedure establishes how executive leadership conducts management reviews to evaluate the performance of the quality management system. It includes assessing opportunities for improvement, determining the need for changes to the system, and reviewing the quality policy and objectives. Delivered in editable Word format for easy customization. Additional support is available for upgrading or adjusting procedures, and consultancy services can be arranged flexibly via email, Zoom, or on‑site visits. For clients requiring full implementation or signed, approved procedures, these services are offered at an extra fee.