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  • Audit Non-conforming work

    Asking about ISo17025:2017 clause 8.2.2 how to implement in a laboratory?

  • Transition from ISO 17025:2005 to ISO 17025:2017

    I am working as an Assistant Management representative in a Quality testing lab that is previously ISO17025:2005, now I need transition to 17025:2017, what mandatory documents I have to prepare and how to prepare a quality manual?

  • Scope definition and its implications

    "My company is a chemical manufacturing company producing products for a wide variety of industries out of a single location, A customer of ours in the cosmetics sector has requested we achieve both the ISO 9001 certification and the EFFCI GMP. My question is are we able to limit the scope to the production of the specific chemistries we are producing for this customer or does it have to be inclusive of all products produced at the facility?”

  • Identifying the method and scope of audit

    ... visera.co/ISO17025Toolkit" target="_blank" rel="noopener">https://advisera.co/ISO17025Toolkit, where there are there is a procedure, audit program format, an audit checklist, and report forms to guide you.

    Also have a look at the articles ISO 9001 Horizontal audit vs. vertical audit at  https://advisera.co/HorizontalVsVerticalAudit and ISO 17025 Technical internal audit: The basics at https://advisera.co/17025TechnicalAudit

  • Fulfilling ISO/IEC 17025:2017 8.9.3

    If you're struggling with documentation, the ISO17025 documents available on documentationconsultancy.com could save you a lot of time. Their toolkit is super helpful for getting started with compliance!

  • Sampling in coal mine

    ... visera.co/ISO17025Toolkit" target="_blank" rel="noopener">https://advisera.co/ISO17025Toolkit where there are there is a procedure to guide you (Sampling procedure) and forms for a  sampling plan and sampling report. Also, have a look at the Clause-by-clause explanation of ISO 17025:2017 https://advisera.co/17025ClauseByClause

  • Food Packaging Testing

    ... 7025:2017 at https://info.advisera.com/17025academy/free-download/checklist-of-mandatory-documents-required-by-iso-17025 Then have a look at what the toolkit can offer to assist with requirements of internal audits https://advisera.co/ISO17025Toolkit

  • ISO 17025 latest version

    If your question relates to laboratories that are currently accredited to ISO 17025:2005, currently the certificates of accreditation to the 2005 version are valid; however accredited laboratories must transition before their certificate expires or by the latest, 1 June 2021. Accreditation bodies will arrange assessments against ISO17025:2017 before the deadline. That means that they need to be in the process of meeting ISO 17025:2017 requirements; thus making the old version of the Standard obsolete.

    If you are busy implementing ISO 17025 and have not yet applied for accreditation, then no, ISO 17025:2005 is not applicable. The laboratory must implement to meet ISO 17025:2017 requirements.

    For further information see

  • Team training in Good Manufacturing Practices - is it essential?

    ... t is essential to educate employees that are directly involved in manufacturing the medical device - workers in the production, workers in the warehouse, workers in the quality control, cleaning staff. Also, some management staff also need to be educated to know how premises have to be organized (eg. to avoid cross-contamination), what resources it is necessary for the smooth implementation of GMP, what knowledge it is necessary to ensure for smooth conduction of GMP.

  • Distance between people in calibration lab

    ... from the ISO17025 Academy at https://info.advisera.com/17025academy/free-download/project-plan-for-iso-17025-implementation
    The ISO 17025 Toolkit at https://advisera.com/17025academy/iso-17025-documentation-toolkit/
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