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Mar 5, 2018 - A2LA uses as the basis for all of its accreditations (of both testing and calibration laboratories) ISO/IEC 17025, “General requirements for the.
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More Information Description: ExtraISO/IEC specifies the general requirements for the competence, impartiality and consistent operation of laboratories.ISO/IEC is applicable to all organizations performing laboratory activities, regardless of the number of personnel.Laboratory customers, regulatory authorities, organizations and schemes using peer-assessment, accreditation bodies, and others use ISO/IEC in confirming or recognizing the competence of laboratories.Pages38PublisherISO.
Hello People,i agree with the view that it is advisable to have a Quality Manual in place as it is the basic document for introduction of the lab. Secondly would also suggest that the Procedure manual (prepared in lieu of 2005 standard requirements) be kept intact or upgraded. This will ensure that the process is cascaded to all levels.in the recent interactions that i have had with a few auditors, it was evident that all audits will now be objective. Irrespective whether you have a documented procedure or not, it has to be verified.now i wanted to enquire whether there are any templates available for preparing the Quality manual as per 2017 requirements.
Hello People,i agree with the view that it is advisable to have a Quality Manual in place as it is the basic document for introduction of the lab. Secondly would also suggest that the Procedure manual (prepared in lieu of 2005 standard requirements) be kept intact or upgraded. This will ensure that the process is cascaded to all levels.in the recent interactions that i have had with a few auditors, it was evident that all audits will now be objective. Irrespective whether you have a documented procedure or not, it has to be verified.now i wanted to enquire whether there are any templates available for preparing the Quality manual as per 2017 requirements. I am sorry for the delay in this response.Do you have a copy of the standard? Indicates no requirement for a Quality Manual exists in ISO/IEC.Why have a manual if none is required for accreditation?
You can document procedures, scope, policy and anything else your lab and the standard requires. You could have a booklet-sized central source in which these documents are gathered. I have also seen them as tabs in a spreadsheet document.I have seen a table of contents essentially used as a Manual. If you use a process map, the procedure references could be listed there. I have also seen procedures referenced as part of actions to address risks, in documentation where risks are listed. There are many practical methods to replace a Manual that frankly was historically used by very few people.All of that said, if you must have a Manual, there are. I agree with Andy that their usefulness is limited, hence my points above.