ISO/TR (en), Guidelines for quality management system. . Título: Esta Versão Corrigida da ABNT ISO/TR de , incorpora a Errata . Direct link NBR ABNT iso tr free pdf ISO TR – Diretrizes para a documentacao de sistema de gestao da qualidade(1).pdf. ISO/TR. (E). PDF disclaimer This PDF file may contain embedded typefaces. In accordance ABNT ISO/TR um guia para a.

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ISO TR 21074-2016

Laboratory Process Control – 4. The Task Force is confident that QS, implemented in the spirit of continuous improvement, will enhance quality systems while eliminating abbt requirements and thus reducing costs. Electronic Communication – 4.

Progress toward the plan should be tracked. Where a qualified laboratory does not exist for a given piece of equipment, calibration services may be performed by the original equipment manufacturer.

All production tooling shall be in place and running at full production feeds and speeds, utilizing all regular production direct and indirect personnel and support systems. Trends in customer satisfaction and key indicators of customer dissatisfaction shall be documented and supported by objective information.

Metrological confirmation system for measuring equipment. All QS requirements shall be addressed in the quality system documentation, but not necessarily by individual procedures. Maintain a listing of their QS qualified auditors.

The supplier shall review and approve purchasing documents for adequacy of specified requirements prior to release. Xbnt corrective or preventive action taken to eliminate the causes of actual or potential nonconformities shall be to a degree appropriate to the magnitude of problems and commensurate with the risks encountered.


Affordable Care Act Updates: Quality System Requirements Categories, added.

Quality System Requirements – AIAG Manual_百度文库

A serial number traceable to the device calibration record meets the intent of this requirement. QS is an input document for development of a quality manual. Diamonds also highlight important characteristics on fixtures and gauging procedures during design verification, product validation, or revalidation.

Machine setup, die change and machine changeover times?

Unique symbols identifying safety and regulatory characteristics on components designed by other companies e. The description of nonconformity that has been accepted, and of repairs, shall be recorded to denote the actual condition. The supplier shall eventually dispose of records.

Guide the implementation of fre quality system. These instructions shall be accessible at the work station.

These have been well received by the supplier community and their success served to encourage additional efforts. Last-off part comparisons are recommended. See Annt Laboratory Requirements 4.

ISO TR 20173

Pertinent quality records from the subcontractor shall be an element isp these data. They continue to be developed and can be very useful when difficult situations or when Quality Managers and Consultants need a reference document for back-up to their recommendations. There is no specified checklist that MUST be used for internal auditing purposes. Third party auditors shall identify opportunities for improvement e.

Each customer will continue to develop unique supplier ratings. The Second Edition may continue to be used until January 1, at which time it becomes obsolete, unless otherwise notified by the customer.


Accept product Continue to reduce process variation. Advanced Ido Quality Planning – 4. Job setups shall be verified whenever a setup is performed e. Tier 2 and below. Purpose QS defines the fundamental quality system expectations of Chrysler, Ford, General Motors, Truck Manufacturers and other subscribing companies for internal and external suppliers of production and service parts and materials.

Would vree like to tell us about a lower price? Be the first to review this item Amazon Best Sellers Rank: Verification of conformance to ISO or ISO for suppliers that are not responsible for the design of any product supplied to any customer subscribing to this document is a necessary condition for registration to QS Approved Materials for Ongoing Production – 4.

Norma Abnt ISO – PDF Free Download

Prototype – a description of the dimensional measurements and material and performance tests that will occur during Prototype build see APQP reference manual. Design failures shall be documented in the validation records. NAO Suppliers shall verify that they are using the latest version of these documents at least annually.

Modified Rr Control Requirements4. Any such product that is lost, damaged or is otherwise unsuitable for use shall be recorded and reported to the customer see 4.