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.
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
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?
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?
What are the procedures for validation and verification of methods, how to apply it, also what's procedure for personal competence?
Please help me for how I can apply the different forms and tamplets for example risk and apportunitious ...please give me example
I wanted to see if you build Meas of Uncert budgets. I currently calibrate pipettes, but not accredited. Looking to get accredited and wanted to see if you build the budget. We do have Type "A" data, and all equipment to include balance, software, environmental, etc...