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.
Ana Rita Pires
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Ana Rita Pires is a PhD student at the University of Porto (Portugal).
Articles by Ana Rita Pires
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- Obtaining simultaneous multiple dissolution profiles of solid oral dosage formulations
Published: May 1st 2010 | Updated:
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