Testing the dissolution rates of a pharmaceutical formulation (also known as in vitro availability) aids drug quality control and is a compulsory requirement of the British, European and US pharmacopoeias.
D. López Malo
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D. López Malo is junior researcher at the Department of Analytical Chemistry, University of Valencia (Spain).
Articles by D. López Malo
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Latest Updated Articles
- Obtaining simultaneous multiple dissolution profiles of solid oral dosage formulations
Published: May 1st 2010 | Updated:
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