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Writing quality manual and nominating quality manager when we implement ISO 17025:2017
Good evening As the previous standard there mentioned about the Quality Manager and Quality manual, but in the new version even 9001 and 17025, no mentioned about QM and Q. manual I saw new quality manuals for some companies and institutes according to 9001:2015 or 17025:2017. Can we write a quality manual and nominate a quality manager for our institute, when we implement ISO 17025:2017? -
ISO/IEC 17025:2017 accreditation timeline
We are vetting an opportunity to expand our lab for Heavy Metal testing and pathogen testing (salmonella). What type of timeline would you suggest after a lab is fully operational including ISO/IEC 17025:2017 accreditation? Best guess in getting a lab certification set up? I’m assuming some amount of time before lab is operational to get application data submitted and then some amount of time after lab is operational to validate procedures, processes, etc. and then finally third party validation. Is this a fair assessment? Any help would be much appreciated. Other recommendations? I noticed that the site mentions familiarity training. Are you all an approved certified body for ISO17025 audits? -
ISO 17025 first steps
I'm a master student doing an essay about a company wanting to get it's laboratory accredited, in sampling an calibration.
my question is if they have iso9001 certificate for the whole facility is the laboratory included or it needs it's own SMQ? -
Methods verification
I would like to ask you about methods verification (we have implemented standard methods), so we don't have to validate them but only verified. Which parameters will be verified for standard methods? About quality data control, which procedure can you suggest to me?
If you have some examples or some specific information about that and if you can send me something I will thank you very much.
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Calculating uncertainty
Please help me in calculating uncertainty and how can use uncertainty to evaluate the competence of the operators and also that the method is fit for purpose
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ISO/IEC 17025:2017 & ISO/IEC 17020:2012 certification
If a company is already certified in the above mentioned ISO standards, what do they need to do in order to maintain their certification? Is there a requirement to update to the latest iteration? If so, how often do they need to do so? -
ISO 17025 implementation
Please can you clarify the document " ANNEX 2 OF THE OMCL NETWORK GUIDELINE “QUALIFICATION OF EQUIPMENT” QUALIFICATION OF GC EQUIPMENT " we have our SOP and we have read all documents and checked our SOP regarding to the documents but we cannot decid if there is major differences?
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ISO 9001:2015 vs ISO 17025
When a testing laboratory is ISO 9001:2015 certified, what requirements are not met for 17025? We are 9001:2015 certified, but comparing the two standards, it seems that we meet all the requirements of 17025. Is this correct?
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Procedures for validation and verification of methods
What are the procedures for validation and verification of methods, how to apply it, also what's procedure for personal competence?
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Accreditation for ISO 17025
Please help me for how I can apply the different forms and tamplets for example risk and apportunitious ...please give me example