Automation of dissolution tests

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Automation of dissolution tests

Dissolution testing of drug formulations was introduced in the 1960s and accepted by health regulatory authorities in the 1970s. Since then, the importance of dissolution has grown rapidly as have the number of tests and demands in quality-control laboratories. Recent research works lead to the development of in-vitro dissolution tests as replacements for human and animal bioequivalence studies...

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ژورنال

عنوان ژورنال: Journal of Automated Methods and Management in Chemistry

سال: 2003

ISSN: 1463-9246,1464-5068

DOI: 10.1155/s1463924603000026