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Can you please verify: do we audit all processes 1 time for every 3 years (=3 times in a 3-year cycle) or is it only 1 time in 3 years?
It states that we have to audit all processes over a 3 year cycle/audit program/period.
Do we audit all process each year during the 3 years, which would equal 3 audits per process or,
Do we audit 1 time during the 3 year period so each process is audited 1 time in 3 years?
I am trying to get clarification on the requirement.
I believe, and in my past experiences, I have audited all processes each year in a 3 year cycle, so each process is audited 3 times in the 3 year cycle.
(in other words each process-full QMS processes must be audited every year)
The question has arrised at my new place of employment, but the standard is not clear.
Happy new year everyone!
i'm wondering what indicators which commonly used to mesure the performance of the industrialization process which includes APQP procedure and the PPAP file submission
thank you for your help!
Is it a requirement to have a list of mandatory procedures in the quality manual?
My most pressing question is what are the most relevant tools supporting PPAP processes? The reason for this is that I am creating an outsourcing team and I need to be sure we are teaching the most relevant tools regarding PPAP
1. IATF16949 dokumanlarını biliyorum ancak ISO9001:2015 ten farkını çıkaramadım. ISO 9001 de olmayıp IATF16949 olan neler var nereden ulaşabilirim bu bilgiye.
2. Ve ISO 9001:2015 de tasarım iatf16949 gibi hariç tutulabiliyor mu acaba şimdiden teşekkürler ?
Is IATF define the time limit for document show to the auditor during audit
If Yes then in which clause?
'm trying to figure out what to ask during an audit regarding this portion of clause 184.108.40.206 h) defined responsibilities, definition of escalation process and flow of information, including top management, and customer notification;Thank you.
Company where I work is not very big and activity is related with assembly of wire harnesses for automotive.
Recently I was requested to give info for Lifetime of the product and Warranty management to our OEM potential customer I have read of course IATF points related to this but it's still not very clear.
1. What are obligations related to warranty management from supplier side?
2. What info I have to collect to answer about lifetime?