Hello all,
I work in the pharmaceutical lab as a quality officer, I prepared SOP for risk management according to ISO 31000:2018 and I need help to link it with ISO 17025, I attached the SOP to advise me. Thanks
From an ISO 17025 standpoint, there are a number of risk-based activities:
-Sampling Plans
-Measurement Systems Analysis
-Calibration frequency
-Procedure for monitoring the validity of testing and calibration
-Internal audit schedule
From an ISO 17025 standpoint, there are a number of risk-based activities:
-Sampling Plans
-Measurement Systems Analysis
-Calibration frequency
-Procedure for monitoring the validity of testing and calibration
-Internal audit schedule
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