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ISO and quality management

IATF 16949 Sanctioned Interpretations 1–15 — 2018 archive

2018-11-20 03:48:53 | Lượt xem: 5283 | ISO and quality management

On 12 November 2018, IATF published an updated set of Sanctioned Interpretations incorporating SIs 14–15.

The document IATF 16949:2016 – Sanctioned Interpretations #1–15 provides access to interpretations issued by IATF during 2017–2018. A short reading guide and a link to the English document are provided below.

Archived document: SIs 1–15 are not the latest complete set. Before implementation or an audit, check IATF’s official SI list, effective dates and subsequent revisions.

Download SIs 1–15

Download IATF-16949-SIs_Oct-2018_12Nov2018 — English PDF

Illustrative image, not a photograph of an actual project.
Illustrative image, not a photograph of an actual project.

What is a Sanctioned Interpretation?

A Sanctioned Interpretation changes how a rule or requirement is interpreted and can become the basis for identifying a nonconformity. Reading only the original standard without considering effective SIs may therefore lead to outdated implementation.

Publication milestones in the archived document

  • SIs 1–9: issued and effective in October 2017.
  • SIs 10–11: issued in April 2018, effective June 2018.
  • SIs 8 and 10: revised in June 2018, effective July 2018.
  • SIs 12–13: issued in June 2018, effective July 2018.
  • SIs 14–15: issued in November 2018, effective January 2019.

Quick guide to the 15 interpretations

  1. Customer requirements: clarifying who determines requirements when vehicle manufacturers and associated entities are audited.
  2. Product safety: clarifying special approvals for requirements or documents containing safety-related information.
  3. Contingency plans: considering disruption from cyberattacks alongside equipment, supply and infrastructure risks.
  4. Internal auditor competence: distinguishing system, manufacturing process and product audit competence, and retaining evidence of trainer competence.
  5. System documentation: showing where customer-specific requirements are addressed; a matrix is one possible format.
  6. Special characteristics: linking identification and controls across technical documents, risk analyses, control plans and work instructions.
  7. Control of external provision: clarifying responsibility for characteristics that pass through the system without inspection by the organisation.
  8. Supplier management system development: establishing minimum and target levels based on risk, eligibility and customer requirements.
  9. Concession approval: clarifying when customer approval is required for a product or process that differs from its current approval.
  10. External laboratories: reviewing competence, accreditation scope and evidence of customer acceptance under the SI.
  11. Temporary changes to process controls: managing alternative methods where applicable, without assuming that every primary control must have a backup method.
  12. Process effectiveness and efficiency: clarifying management review responsibilities and selection of appropriate measures.
  13. Management review inputs: connecting quality, process, customer and maintenance results with relevant risks.
  14. System auditing: managing the programme over the three-year cycle specified in this document, with each process’s frequency based on performance and risk.
  15. Embedded software: distinguishing software that controls an automotive component’s functions from software controlling manufacturing equipment.

How to use the document in your organisation

  • Read each relevant SI in full in the official document, rather than relying only on a summary.
  • Compare the effective edition against your processes and customer-specific requirements.
  • Assign responsibility for documentation updates, training and verification of implementation evidence.

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