Risks of Validating Sampling during Quality Supervision and Inspection of Drugs
2013
The time limit and requirements for sampling according to Drug Quality Supervision and Inspection Regulations were discussed and potential risks of sampling during quality supervision and inspection of drugs were analyzed.Validation was regarded as indispensable for collected samples.Sampling should be enhanced in the process of manufacture,marketing and use to ensure the combination of inspection sampling with daily administrative supervision.
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KQI