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How do monitor integrity issue in QMS in a utility firm?
If you are starting to work for a new company that is wanting to become ISO 9001 Certified, where do you start?
My understanding is that ISO 9001:2015 allows significant latitude for organizations to determine the extent of process documentation they feel is required to maintain their QMS. However, it seems like trying to navigate a certification audit with very sparse process documentation would be to say the least challenging. The small to medium sized company I represent has very sparse process documentation and I am concerned about our odds of successfully navigating the certification audit. What are your thoughts or recommendations?
I need your advice and guidance on how to write ISO 9001 on production/services requirements records for my company.
What about the people aspect of ISO?
I wanted to have an organisational chart about the structure of a chemical laboratory.
I am working on it, however, feel that I am missing things in it.
Can you help?
Concernant le domaine d'application, est-ce obligatoire d'avoir une information documentée spécifique décrivant les limites du SMQ même si on a déjà mentionné le domaine d'application dans le manuel qualité?
Que faire pour satisfaire à un audit ?
Para que sirve los estudios de riesgo y cual es el beneficio?