ISO 9001 - Expert Advice Community

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  • Time for implementation

    "We want to be ISO 9015 certified by next year. However, we need to go through reviewing and documenting all our processes since it has not been updated for so long. May i ask if you can possibly give me some insight on how long each stage of activity will take before we get certified? A sample timeline will be most helpful.”
  • Set up a new QMS

    "How to set up a new QMS for an organization hoping to get ISO 9001:2015 certification?”
  • Monitoring, measuring, analyzing and evaluating

    "How do you monitor, measure, analyze and evaluate data and information and also identify different of means of analyses with relevant templates”
  • Auditing a production area

    “I work in... water bottling factory. Our ISO 9001 certification audit is on 23rd April. Can you help me what aspects are important to consider on the production area? Including the SOPs.
  • 5S and ISO 9001

    "Do you have awareness on Good housekeeping (5S) as part of the QMS”
  • Reviewing documentation

    1. We review the Quality policy in our MRM meeting every year, so do we have to update the date on the Quality policy as well as when it was last reviewed?
  • Drawing control

    “Do drawings or technical illustrations need to be controlled (i.e. have a control stamp) or require any specific format?”
  • Integrating management systems

    “I want to know how the different ISO standards can be integrated to have an integrated system?”
  • Mandatory procedures and content

    1. Documenting procedures. Is mandatory to document each and every procedure we carry out in our organization?
  • Clause 4.4.2 and processes

    My question is, to Standard Clause 4.4.2...when it speaks to "support the operation of its processes", is that meant to maintain documents on ALL company processes involved in creating a product or is that requirement isolated to only maintain documented information for the operation of our "Quality" processes?”