Please select user.
There are no topics yet.
There is a debate about the recalibration date, we perform our plan on monthly basis & the auditor insists to be done by day, so the calibration validity ends by the cal. month 1st.date. which method is more accurate?
I come from a cGMP background so DQ/IQ/OQ/PQ is standard for all equipment, but now I'm trying to set up an ISO 17025 compliant lab and am not sure if I need to do the same qualification. Would calibration and verification to make sure the equipment is functioning (using a lab developed reference standard, if CRM is not available) suffice?
Can you help me to found more reference about Measurment uncentrity .?
What are the best methods and procedure on handling samples according to International best practices. Example waste water (effluent) and potable water)?
Hope you are doing well,
Actually, I need your help to find the accurate and the most clear difference between validation and verification on the laboratory.
I really appreciate your answer.
Thank you for your time.
How to properly implement section 7.2 and 7.6 for a microbiological lab?
Please explain further sub-clause 6.4.2 for our reference.
Hi, I am revising my Quality Management Plan to include risk. How specific should certain risks be detailed in the QMP?
1. What is the difference between certification and accreditation?
2. I do not understand the concept of measurement uncertainty.
Can you help me with it?
3. I do not understand clause 6.5 Metrological traceability.
What do they mean by the measurement uncertainty of each calibration must be available?
I am a quality manager and i have to perform an internal audit using the guidelines of iso17025:2017. Do you have any guidelines and tips to excel in this audit?