In the manufacture of solid dosage forms, the rate at which the active pharmaceutical ingredient (API) is dissolved into solvents simulating the digestive tract fluids is determined with dissolution ...
Rockville, Md., April 1, 2008 — The U.S. Pharmacopeial (USP) Convention today announced results of a study comparing the dissolution variability of USP Prednisone Lot P Reference Standard tablets to ...
A fully automated dissolution lab is an integrated, end to end architecture that enables reproducible testing, continuous ...
A traditional dissolution cycle is a multi-step process involving apparatus setup, media preparation, sample loading, timed ...
In order to highlight the importance of dissolution testing in pharmaceutical industry as a tool in drug development and quality control, Society for Pharmaceutical Dissolution Science (SPDS) ...
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Cholesterol medication recalled over ‘failed dissolution specifications’: What to know
Over 141,000 bottles of cholesterol medication have been recalled due to “failed dissolution specifications,” suggesting that ...
The dissolution profile of inhaled drugs underpins therapeutic efficacy and is an area of increasing regulatory scrutiny, particularly for the demonstration of bioequivalence in a generic. The new ...
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