Introduction to supplier audit

Our supplier audit service includes detailed analysis of the entire supply chain to ensure that it is always open and transparent to the company and customers. The second party audit service evaluates whether the supplier meets the established requirements. Identifying gaps and improving opportunities is crucial for professional supplier management. The NCE supplier audit service can provide valuable support for the selection and evaluation of existing and new suppliers.

Supplier audit provides a strong guarantee for your business reputation and supply chain through NCE audit and verification services. Supplier audit, that is, the second-party audit, is the audit of suppliers by customers, which helps to confirm that suppliers provide services and products according to your requirements or agreements, and helps your business network improve the resilience of the supply chain.

Our supply chain audit service (also known as second-party audit scheme) enables you to have a comprehensive understanding of the operations of your global suppliers. Our expert team has developed a supplier audit plan that suits your specific requirements and combines it with our risk data and analysis, so that you can conduct a comprehensive risk-based audit of supply chain operations.

Supplier's approach
Supplier audit application

As one of the nationally recognized audit institutions of medical device management system standards, we have the professional knowledge to provide supplier audit in a wide range of recognized fields. If properly managed, supplier audit can improve business performance and support sustainable development. Your entrustment, we will arrange an experienced NCE auditor in your location to verify that your supplier's business information, policies and procedures meet your organization's requirements and objectives in all aspects, including:

ISO14971 introduction and operation of risk management system
ISO13485 introduction and operation of medical device quality management system
Introduction and operation of regulatory requirements such as medical device Good Manufacturing Practice
Understanding and implementation of medical device regulations
Stability of product quality and business continuity