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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...
Please advise,
I thought that a procedure was not needed for ISO 17025"2017 for documents and records. I don't believe they are mandatory according to the requirements but wanted to verify.
If a new equipment didn't bring any certificate of calibration, can I use the receipt as first use proof for a specific as valid calibration?
Do you have any suggestion for accreditation bodies for Lab to accredited ISO 17025?
What is the difference between accreditation bodies and certification bodies?