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Your question is very particular and I only can give general answers because each case is a case and I don’t have enough information. Nevertheless, I would say that you can eliminate those databases from your QMS intranet. After that you will still control the information about your parts and product list (name, reference, version, change control, approval, distribution, obsoletes).
The following material will provide you information about document control:
ISO 9001 – How to set up document approval/withdrawal within your QMS based on ISO 9001:2015 - https://advisera.com/9001academy/blog/2016/04/12/how-to-set-up-document-approvalwithdrawal-within-your-qms-based-on-iso-90012015/
free on line training ISO 9001:2015 Foundations Course – https://advisera.com/training/iso-9001-foundations-course/
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Dec 10, 2017