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iso-9000-terminology-headline

ISO 9000 is a series of standards, developed and published by the International Organization for Standardization, that define, establish and maintain an effective quality assurance system for manufacturing and service industries.

Common ISO Definitions

Accreditation

The act of giving an organization formal approval to operate an audit and registration program.

Auditor

ISO auditors perform assessments and surveillance. They are the “front line” people during an audit. An internal auditor is normally an employee who is trained in auditing and, depending on the company requirement, carries out annual or bi-annual audits. External audits are carried out by a company not affiliated in any way to the organization being audited.

Concession

The formal act of yielding, waiving, or surrendering a right or privilege. A concession is often made in writing by a customer when it has been determined that a product or contractual requirement cannot be met in a practical or cost-efficient way and that dropping the requirement will not materially affect the desired outcome.

Corrective Action Request (CAR)

In the ISO arena, a CAR is by far one of the most frequently used terms for corrective action. The essence of a CAR is to investigate a problem that already happened and requires root cause analysis and resolution to prevent a recurrence.

Discrepancy

A failure to meet the specified requirement, supported by evidence. Also can be called “nonconformance” or “deficiency.”

Document Management System (DMS)

Software used to track and store electronic documents. Capable of keeping track of the different versions modified by different users.

Fault Tree Analysis

The process of identifying potential design weaknesses using a logic diagram that depicts basic faults and events that can lead to system failures and safety hazards.

Observation

Think of this as an area of improvement. An “observation” is a statement of fact made in an audit team’s report. It indicates an audit finding that doesn’t rise to the level of a nonconformity (i.e., no objective evidence of nonconformity, doesn’t require corrective action, etc.) but which, if left alone, could result in a future audit finding.

Policy

A definite course or method of action to guide and determine present and future decisions. ISO mandates a Quality Policy be developed and used as a basis for your quality objectives.

Preventive Action

An action is taken to eliminate the causes of a potential nonconformity.

Procedure

A particular way of accomplishing something; an established way of doing things; a series of steps followed in a definite regular order. It ensures a consistent and repetitive approach to action.

Quality Audit

Examination of an organization’s quality management system to assure conformance to a specific quality standard, such as ISO 9001.

Quality Manual

A document in which your quality standards are described and where your Quality Policy is stated

Quality Management System

A collection of business processes focused on achieving your Quality Policy and quality objectives.

Registrars

Organizations that issue ISO certification.

Verification

The act or process of confirming the accuracy or existence of a systematic, objective, and documented process that conforms to various requirements, such as customer or regulatory requirements.

Validation

The process of establishing that the audit results not only meet requirements but also satisfy the intended purpose.

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