The ISO internal audit will assess the compliance of your organization’s quality management system to the applicable ISO standard and your organization's overall QMS performance. The results are a detailed audit report that identifies nonconformances, observations, opportunities for improvement and strengths. Each nonconformance will contain an explanation of the nonconformance and what is needed to bring your system in compliance.

The Internal quality audit is conducted to ensure ongoing compliance with requirements of your QMS standards, Division's policies and procedures. This is accomplished by auditing against all identified key processes and areas, and by applying all applicable sections of the ISO standard. The results are a detailed audit report that identifies nonconformances, observations, opportunities for improvement and strengths. Each nonconformance will contain an explanation of the nonconformance and what is needed to bring your system in compliance.

The implementation of a certified ISO quality management system will begin with a detailed gap analysis of your current QMS to the ISO requirements. Following the gap analysis we will begin a 12-phase implementation process to bring your QMS system into compliance with the applicable ISO standard. The implementation process can take from 4 months to 9 months to complete. Once full implementation is achieved your organization is to ready to schedule an ISO certification audit.

In the scope of the Supplier Audit, independent auditors visit your supplier’s manufacturing facilities to analyze their manufacturing capacities, quality management system, structural safety, social compliance or environmental impact. This is the best way to obtain a full understanding of your supplier’s business and policies, and receive all the information you need to take any necessary corrective actions.

Supplier audits can be conducted to a number of ISO standards, or your in-house policies.  We can audit your existing suppliers or your potential suppliers.