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1. I have a question about achieving ISO 17025 accreditation for a specific lab at fixed premises. Once you attain accreditation for a lab can you also expand the accreditation to another premises? Would the lab tests being performed in the new premises have to be re-validated etc?
2. Another question regarding calibration due dates. Is it ok to write a calibration due date on a calibration cert for a device we have calibrated? Do we need to write a disclaimer saying the calibration interval is determined by the customer? I've seen this on a number of ISO17025-accredited certificates.
3. One last question, we use a subfraction of an ISO 12103-1 standard dust for calibrating our dust monitors. Does this material need to be tested (particle distribution) by an ISO 17025 accredited laboratory? we have a particle distribution from a non-accredited lab for the material. I am concerned that as we are using it as a reference material we would need to have an accredited certificate of the particle distribution.
I was wondering if you could assist. I’m looking for a check list of sorts to be able to determine what I would need to do in my department to see if we should become ISO17025. Is that something that exists? I’m not looking to go on a course to find that out. I’m more on a fact finding mission at the moment.
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I am still busy with my process of ISO implementation. Can you please assist me with the following question:
Do I have to have any safety courses, CPR or first aid as part of accreditation?
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