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- Stage-I audit is to assess the adequacy of your system in terms of its documentation & structure. Whereas Stage – II audit is on site certification audit.
- Submit details of QMS / its documentation for initial review of documentation by CVI Lead Assessor.
- On completion of documentation review, Veritas CVI certifications shall send you documentation review report indicating short comings if any and allowing you sufficient time to make modifications in the system to meet the adequacy requirements.
- Once you are ready for stage-II audit, you shall intimate Veritas CVI Certifications . so that the audit team is formed and notified to you along with Audit Plan for this audit.
- On the agreed date the certification audit is performed as per requirements of the applicable standard and scope of the audit as agreed earlier. However, befor start of the audit, an Lead Assessor shall once again confirm the scope of audit from you at the time of opening meeting.
- On completion of certification audit, Lead Assessor shall declare findings of audit during closing meeting and would confirm to you if he is recommending your organization for grant of the certificate.
- Always remember that it is prerogative of CVI to grant the certificate. Validity of the certification is for three years subject to your passing the initial audit and two subsequent surveillance audits conducted with in 7-11 & 19-23 months of certification audit.
- When you are nearing completion of 3 years of certification, you may apply again for re-certification.
