Dissolution
USP
Dissolution testing is a crucial process in pharmaceutical development and quality control of solid dosage forms. It measures the release rate of the active ingredient, providing information about the drug product dissolution profile and biowaiver.
We offer both manual and automated dissolution single point and profile analysis as per USP <711> or as per client’s specific method.
Dissolution are equipment with both apparatus 1 (baskets) and Apparatus 2 (paddles).