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I am looking for responsibilities of an iso representative. and documents he or he is responsible for keeping and which departments hold varoius records.
During the management review meeting, what am I supposed to talk about to other members of the meeting?
I am struggling with the range of Quality Records. For example, can a website be a quality document for the purposes of marketing and communication?
How to do internal and external process performance measurements? Please give brief details.
How to identify the difference between correction and corrective in nonconformity?
Regarding 4.1 & 4.2, first prepare Issue then intested party for its & make context of organization?
As per ISO 9001, is it mandatory to prepare quality plan? Or which clause I can refer?
I am looking for a list of common risks that all ISO 9001 Quality Management Systems should account for
Is it ok for me to send a copy of my audit checklist to the auditee prior to the audit?