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  • Section 8.5.6

    Referred to section 8.5.6 (control of change) we are planning to implement " management of change procedure". we plan to use this procedure for all changes in IMS (for changes in procedures, company specification or aspects). We will do risk analysis to identify potential hazards and impacts associated with the changes. All discussed with the staff in conjunction with the change send to QA department for registration 
    is it possible to use this section for these purposes and am I correctly understand section 8.5.6?

  • IMS system

    Our company plans to use IMS. I want to clarify who shall be responsible for document registration in the system. QA specialist is responsible for Quality documentations. Who shall take responsibility for EMS and HSE documentation? 
    Could the QA department take overall responsibilities for IMS?

  • ISO 9001 Clause 8.4 implementation

    Please I need your help on how to articulate and implement the requirements of Clause 8.4

  • Excluding clauses of ISO 9001 for a law firm

    I'm working on the implementation of ISO 9001 in a law firm. What clauses of the standard can we exclude? Clause 8.3 (design and development) seems to be quite obvious; but what else could we exclude?

  • ISO 9001 and supply chain control

    Why does ISO9k not focus more on supply chain control? the existing points on supplier management pay no respect to supply chain and BCM as result of issues caused. also, control of fake/fraudulent components during the supply chain is not controlled.

  • Controlled vs Non-Controlled copy

    I have a question for controlled and non-controlled copy, for students who need sop copies training do I stamp with a controlled or non-controlled copy

  • Reviewing and approving suitability and adequacy documents as an office administrator

    How would I answer the request to review and approve my documents for suitability and adequacy as an office administrator? 

     

  • ISO 9001 Documentation requirements


    Which of the below would be seen as documentation requirements: 1- Quality Procedure, 2-Audit Reports, 3- Quality Manual, 4- Supplier Documents, and 5- Processes with inputs, outputs, interactions & responsibilities?

     

  • ISO 9001

    ISO 9001 is defined as the international standard that specifies requirements for a quality management system (QMS). Organizations use the standard to demonstrate the ability to consistently provide products and services that meet customer and regulatory requirements.

     

  • ISO and six sigma improvement of the service quality of logistics

    How ISO and six sigma can help improve the service quality of logistics?

     
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