This Suppliers’ Control 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 evaluating, approving, and monitoring suppliers to ensure compliance and product quality. Digital delivery within 24 business hours.
This procedure ensures that suppliers are controlled and monitored to meet regulatory and quality requirements. It covers supplier qualification, audits, performance monitoring, and re‑evaluation. 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.