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What are the missing requirements may be reported during auditing as major Non Conformity and minor Non conformity?
How we can cover risk management?
We manufacture measuring units for industry and of course we calibrate our instruments before we ship then as well later on. So we are a calibrating lab...
There is a special 17025 part that is for calibrating laboratories... what is it called?
Do you have any ITP's for fabrication and welding available? I am looking for a couple of ITP's also ISO set up already.
Would you prioritize the implementation of ISO 9001 over ISO 17025 in the laboratory?
Is there any accreditation for a Calibration Company wherein rendering following services; 1.) Storage Tank Calibration 2.) Flow Meter Calibration
We need to do test that requires that they are doing under a laboratory quality management system compliant to ISO 17025 or alike standards. We are both ISO 9001and 13485 certified and my question is if is also needed to be ISO 17025 certified or is this covered by the other two?
Is it compulsory for the laboratory to have statements of conformity and decision rules.
What parameters are important when analyzing samples in an iso accredited laboratory?
i work in a medical diagnostic facility with imaging, physiotherapy and medical lab processes, now we have established a molecular lab, which iso certification can i get the molecular lab certified meanwhile we are currently we are certified to 9001:2015
I got a NON- CONFORMANCE because our objectives were not clearly indicated if they were fulfilled or not. And now I need to write a root cause analysis. What should I include when writing the report?