Write a quality manual

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It might be an important part of your quality documentation. This is called 'documented information' in the current version of ISO Confusingly, they have also decided to use the same term for what were formerly called 'records' - those things that showed what had been done, such as registers, logs, competed forms, reports, meeting minutes and so on. A system must be documented to achieve ISO certification, because having certain documented information is required by the Standard. What can confuse people is that actually you can choose what your documents look like, what format and structure you use, and what to put in them. Provided you meet these requirements.
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How to write the IATF 16949 Quality Manual

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Quality Manual and Quality Policy : Pharmaceutical Guidelines

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Quality Manual Template + ISO 9001 Toolkit

ISO checklist. Help Contact Us. Which Is Right For Me? What's Included?
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Quality Manual and Quality Policy Quality manual and quality policy is a major part of pharmaceutical quality system. A strong quality policy shows the commitment of the company to manufacture the world class quality products. Ankur Choudhary Print Question Forum 1 comment.
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07.04.2021

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08.04.2021

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