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Overview
Compliance
Requirements
Process
Select a Registrar
Draft and Approve
Documents
Conduct Internal
Audits
Complete
Training
Record Corrective
Actions
Conduct Final
Audit
Requirements
Updates
Standards
Glossary
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It
is necessary for an organization to address nonconforming issues
with its procedures, products and processes. The goal of a compliant
Quality Management System (QMS) is a reduction in corrective action
and certainly a proactive approach to preventive action.
If your organization discovers flaws in its QMS or any part of the
organization that could affect quality, it is necessary to record
a corrective action. A corrective action is a record of the process
involved as an organization seeks to identify, address and resolve
the corrective action or nonconformity. Your organization should
also consider preventive action where corrective actions are monitored
and quality within the organization is watched and preventive measures
are implemented to ensure quality.
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Step: 5
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