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Is it required by ISO 9001:2015 that manufacturing binders on the Production floor — that the Table of Contents are controlled?
My new boss at work thinks it is a waste of time to maintain “controlled” Table of Contents for a binder of controlled docs.
Is there information that I can show my boss?
We have a company claiming to be ISO 9001 certified but we have doubts whether this is true. How are we able to verify?
Una pregunta, en el capitulo 4 que documentos pide, que documentos debemos realizar en el capitulo 4
How to prepare for this audit? First audit after a full three-year certification cycle.
As per the ISO 7.5.3, it mentions to provide a list of external documents – can they be both controlled as well as uncontrolled copies?
The company I work for had the surveillance audit done and there were 2 minor NCs observed. I am trying to understand the Root Cause Analysis for it. The Non Conformance was for Clause 7.5.3.1 and 7.5.3.2. The comment said “List of documents for External documents (Standards, codes, guidelines etc) was not found maintained”). I am looking for probable RCAs for this finding. Could you help me out with that.
I want to know about the documentation process of ISO 9001:2015 QMS for educational Institute
We're preparing for and audit and was wondering if we are required to show an Organization Chart(s) in an ISO 9001 Audit