Impurity profiling in pharmaceuticals
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Impurity profiling in pharmaceuticals refers to the process of identifying, characterizing, and quantifying any unwanted substances (impurities) present in a drug substance or drug product, which is crucial for ensuring safety and efficacy by monitoring and controlling their levels within acceptable regulatory limits; this involves using advanced analytical techniques to detect and analyze the structure of these impurities to assess potential toxicological risks.
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Impurity profiling in pharmaceuticals refers to the process of identifying, characterizing, and quantifying any unwanted substances (impurities) present in a drug substance or drug product, which is crucial for ensuring safety and efficacy by monitoring and controlling their levels within acceptable regulatory limits; this involves using advanced analytical techniques to detect and analyze the structure of these impurities to assess potential toxicological risks.
Bol
Impurity profiling in pharmaceuticals refers to the process of identifying, characterizing, and quantifying any unwanted substances (impurities) present in a drug substance or drug product, which is crucial for ensuring safety and efficacy by monitoring and controlling their levels within acceptable regulatory limits; this involves using advanced analytical techniques to detect and analyze the structure of these impurities to assess potential toxicological risks.
AmazonPages: 52, Paperback, LAP Lambert Academic Publishing
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