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I want to audit our Top Management, however there is no guide for them to audit for ISO:9001 and ISO 14001. Could you help me on the to provide a checklist or a guide?
We added a new facility this year. Our surveillance audit is this coming January. Do we need to do anything now or address it to the auditor in the next audit
I’m interested in your course
https://advisera.com/9001academy/iso-9001-premium-documentation-toolkit/
After doing the course/documentation and completing it who would I go through to audit and certify that it was done and do you know how much that costs. I'm a very small company, just me in my country and 5 developers in XXXX, technically they work for another company but I want to get quality up and thought this would be a good step
Names on documents, like releases/ecr/drawings must have first name on it, is this ISO 9001 requirements? Can you send me more information on it, thx.
If we develop tools, jigs and fixtures for production operations, can we get exclusion for ISO 9001 clause 8.3 for design. Although we get drawings and product specifications from our customers, some time we have to make minor changes in the product because of our process capability constraints . Can we still get exemption for design clause 8.3? please advice
What does Clause 6.2 exactly mean? Does every department of an organization should have a quality objective? Can operational business objective (operational target) be taken as Quality objective for an organization? What does " Organization shall establish quality objectives at relevant functions, levels and processes needed for QMS?
Hola, queremos implantar las tres normas, 9001, 14001 y 45001, en este caso nos surge una duda, queríamos saber qué consejo nos daríais a la hora de decidir si deberíamos integrar en un mismo documento los tres procedimientos siguientes o si los haríais por separado, y que ventajas e inconvenientes le veis a ello. Los procedimientos serían los siguientes: