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10.2 - Laboratory Sampling 111.165 Quality risk management is a

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Description

Quality risk management is a systematic process for the assessment

You must not reprocess a rejected dietary supplement or treat or provide an in-process adjustment to a component

and sanitizing operations

All personnel should be aware of the principles of GMP that affect them and receive initial and continuing training

EP or other recognised test methods

10.2 - Laboratory Sampling 111.165 Quality risk management is aYou must take, without being a source of contamination, representative samples of each dietary supplement that you manufacture, identified through a sound statistical sampling plan (or otherwise every finished batch), before releasing for distribution, to verify that the finished batch of dietary supplement meets established product specifications

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