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First, I would like to thank you for the content available on your side
Let's say, for example, the APQP approach can be implemented for meeting the criteria for design and development and related clause. Do we have a standard approach/Framework for meeting all Quality clauses, which will ensure that efficiency of my process?
sheet metal industries (press shop)process validations, any guidelines?
Is Core Tools the most important tools in implementing IATF 16949? Why?
Do internal auditors need training?
1. My understanding is that IATF16949 primarily applies to an internal manufacturing site, with support functions including design, sales etc being included in the scope. But what if we want to include other design groups in the scope, but their products are not manufactured internally, but at external IATF16949 certified suppliers? Can they be included in the scope? Or can we only include design groups that design products that are manufactured in the certified manufacturing location?
2. If we want to have a Single Manufacturing site certified, but with other internal manufacturing sites includes as extended sites, there are criteria outlined in the IATF "rules" Annex 4 that I would like clarification on: E.g.
We are a steel processor with an ISO 9001-2015 certified company now.
Can I have a single process (stamping) certified to the IATF 16949 standard?
Based on what the sample size to do MSA is fixed like 10 or 30 nos.?
1. Is there a special treatment or additional activities for the IATF audit (Stage 1 and 2) of a new Plant in case there is an on going escalation with a customer happening before the Audit. What are the implications if the escalation is on going during the Audit?
is online internal audit is accepted by IATF external auditors?