Quantitative evaluation of dissolution profiles: From simple approaches to advanced chemometrics
Many forms of drugs are designed to undergo dissolution upon oral administration. The kinetics and efficiency of this process are critical parameters to be controlled. The methods of its evaluation are described in official guidelines issued by the Food and Drug Administration (FDA), European Medici...
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| Main Authors: | , |
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| Format: | Book |
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Pharmaceutical Association of Serbia, Belgrade, Serbia,
2024-01-01T00:00:00Z.
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Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
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| Copy 1 | Available |