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ISO 9001 - Expert Advice Community

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Product: Conformio Product: ISO 27001 Documentation Toolkit Product: ISO 13485 & MDR Integrated Documentation Toolkit ISO 27001 Product: ISO 27001 & ISO 22301 Premium Documentation Toolkit ISO 9001 Risk Assessment Product: ISO 13485 Documentation Toolkit ISMS Internal Audit register of requirements Product: ISO 27001 & ISO 27017 & ISO 27018 Cloud Documentation Toolkit Product: ISO 27001/Risk Assessment Table ISO 9001:2015 ISO27001
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  • New employee in charge of ISO 9001 transition

    I am recently joined with the company and I am sure how they will react to my ideas and suggestion. May be i can pass the documentation only preview, example documents. I have following questions:

  • Gaining competence for ISO 9001:2015

    I would like to know that internal auditor certified by ISO 9001:2008 need to attend ISO 9001:2015 internal auditor training. Do these auditors attend ISO 9001:2015 awareness?

  • Nonconformity and CA

    In the 2015 toolkit, does 12_Procedure_for_Management_of_Nonconformities_CA satisfy requirements for both 8.7 Control of Non Conforming outputs and 10.2 Nonconformity and CA? In 2008 standard we had two separate procedures for 8.3 Control of Non Conforming Product and 8.5.2 Corrective action.

  • Impact of document control on the company

    My question is this, what is the impact of document control on an organisation ?

  • Determining scope of QMS considering context of the organization

    Dear Sir, please advice how to define scope by considering external and internal issues and needs of interested parties as per clause 4.3 of revised standard.

  • QMS in rice industry

    What the requirements and the main elements implementing QMS (ISO 9001) in rice production. What are specific requirements I should do for that and what documents I need?

  • ISO 9001 in hospitals

    I would like to know more about 9001 in hospitals and clinics. What documents we need to prepare before the audit?

  • Prepare for the certification

    Your emails have always been helpful to me in appreciating the process to certification. To start with, thank you for all the emails. My query right now, if I may, is the preparation stage. How would I start from preparation to full certification? Should I need to acquire tools and guidelines, create a committee or propose to document all the internal processes, define each function and align with the standard or all of the above? The bottom line of the question is how I would start before I enter into contract with certification body?

  • Auditing design and development

    I would like to thank you in first for a favour ,and i would ask about main point in design procedure audit and an example if available please

  • ISO 9001 scope and clause exclusions

    Hello. We are a small company, 12 people, less than £1 million turnover. We design our own products, assemble, test and then monitor in the field when bought by customers
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