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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?”

  • How to comply with 7.1.5.3.1.d

    Thank you for the feedback. Let me clarify some points. We had a documented instruction and method defined using weights accredited ISO17025. But the auditor wanted to see that this method was based on international and national process standard (Such as ASTM, EN ...) and find the reference to this process standard in the instruction. And that was not the case.

    Regarding the capability method, I would like to know if referring to the MSA instruction and MSA analysis is enough to fullfill with this requirement. I cannot see any added value to calculate Cgk based on VDA if a complete R&R analysis is already existing based on AIAG MSA

  • ISO 17025 - Traceability Questions

    Hi you asked

    We are planning on being a Testing & calibration laboratory (ISO17025) and would like to issue calibration certificates (for a set of calibration lenses) for use by others as part of the process above, what amendments need to be considered? (we will perform uncertainty budgets etc.)


    You can issue traceable calibration certificates, to be used by testing laboratories provided you demonstrate full technical competence, control, and properly evaluated uncertainty in line with ISO 17025 for your metrology scope.

    This includes, besides ensuring an unbroken traceability chain to NIST

    • Defining your calibration capability (range and uncertainty) 
      Specify the lens power range covered and the uncertainty you can achieve

    • Using validated or verified calibration methods
      Ensure the method is fit for purpose and performs consistently.

    • Developing and reporting measurement uncertainty
      Establish an uncertainty budget (including standards, equipment, environment, and repeatability) and report it with results.

    • Maintaining calibrated and controlled equipment
      Apply a calibration programme with periodic recalibration and checks.

    • Implementing ongoing checks for the validity of results
      Use check standards or repeat measurements to confirm performance.

    • Issuing compliant calibration certificates
      Here you will be guided by your accreditation body. Include results, uncertainty, traceability, and relevant conditions. to meet the requirements of ISO 17025 for reporting calibration results.

  • 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

    ... visera.co/ISO17025Toolkit" target="_blank" rel="noopener">https://advisera.co/ISO17025Toolkit where there are there is a procedure and forms to guide you. Also, read  the article How to perform management review in ISO 17025 at https://advisera.com/17025academy/blog/2021/05/03/how-to-perform-management-review-in-iso-17025/

  • 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
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