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I’m a quality manager and we have an internal audit plane this month what the best procedure to perform Lab. Audit according to ISO 17025 : 2017 in the pandemic of Covid-19 ?
On the other hands what if the lab. Do only verification by blind samples ( quality control ) that they make for lab . instruments and he find the results e corrects and he didn't make calibration as it listed the calibration list period?
I am having a hard time to figure out what I should write in our quality manual and an audit plan, if we wish to use an external company for the internal audit.
I will like to know how to set up a project applying the said standard and the effects of ISO 17025 on projects and how I can obtain a certification for the same ISO. To show competence on potential employers.
1. How should risk assessment be done?
2. And in which areas should the risk assessment be performed?
1. If I can not purchase the last version of the method right now, can I use the old one?
2. If not, what mean of "unless it is not appropriate or possible to do so." in this clause.
I'd like to know if calibration service providers are required by the ISO 17025 standard to provide clients with a calibration recall list for the calibrated measuring equipment.
which clause in ISO 17025:2017 does talk about any exclusion?
hi am about to start implementing my lab quality system. New in the field. am struggling to understand what is the first document to have as a starting point. I established the LMS myself, successfully so. I also need to know if or do I have the option to implement the LMS manually or can I buy or get the software to implement it because it looks like too much work. Please advise.
For initial first gap assessment by Certification body what is the requirements for proficiency testing / ILC and repeatability & repeatability?