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  • Question about tensile testing

    I was informed that only type IV specimens in tensile testing of plastics according to ASTM D638 are accredited by ISO 17025. May I know why that is?

  • Uncertainty calculation

    I need some clarification about uncertainty calculation

  • Laboratory Certifications for ISO9001 and 17025

    One of our customers has mandated ISO9001 and also 17025 in specific areas. Are these two separate certifications or can they be combined?

  • Writing laboratory document and record control procedure

    How can I write for our laboratory document and record control procedure?

  • Completing implementation

    I have  a qeustion and I hope if you could  give me the solution
       In my organization  we have Two systems   the first  is a laboratory system that has been established in accordance with International ISO /IEC  17025: 2017 and is applied and maintained ,this system have a guide to policies and procedures ,and this guide  were mention that the laboratory implements the clause  8.1.2  option A  in ISO  17025 ,  and this guide approved by the  General Director of the organization and the Director of  the Laboratories , this guide  prepared by the quality manager in the Laboratories   and after  we implement   the internal audit  and   the managemet review ,the lab will request  the accredation .

      The second  system  in the organization   were applied  ISO 9001: 2008 ,and the certificate  has been expired  , now  the presentitive of the management  want to transfere to ISO 9001 :2015  , and he  request the quality manger of the laboratories to give him all the procedures and forms to make the code of ISO 9001  ,  is that true or the lab have to  refuse to give the management representitive  the procedures and forms (template) .and complete implemented the ISO 17025 

  • Risk and corrective action

    Dear Ms/ Mr, Hi. I want to know about the risk of the corrective action form and corrective action procedure. An audit tell me that I should consider the risk when I want to write the corrective action? And also I should consider it in the corrective action procedure. Could you please help me?

  • Expired reagents

    What would the standard requires when the laboratory wants to use expired reagents, as management is placing it under clause 6. 4.9 but as Quality commander I do not think it is allowed

  • Are CRM certificates considered external documents?

    Are CRM certificates considered external documents even though you can get them online?

  • ISO 17025 audit

    I have a very barebones understanding of what an audit needs to cover but I lack the experience of knowing how to conduct an audit.

    For example, I know that an ISO 17025 audit needs to look for up to date equipment calibrations, but I do not know the reference guidelines set out in ISO 17025 (clause 7.4 I believe) for this and what would need to be presented as evidence, how to get this evidence or from who.

    In other words I know "what" to look out for, but not "how" to or "who" to.
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