Tablet Dissolution TD122

Drug dissolution testing plays an important role in drug production and is used throughout the development process for quality control testing to assess batch stability, product release, and stability tests. In vitro dissolution testing for tablets, capsules, or other solid oral dosage forms allows for the assessment of the presence of the active pharmaceutical ingredient (API) in the active pharmaceutical ingredient formulation and is an indication of the time required for the drug substance to be released from the dose. Our scientists provide standardized dissolution testing for solid dosage products in accordance with USP (USP) 711, European Pharmacopoeia (EP) and US FDA guidelines. He is experienced in developing specific dissolution approaches that conform to released product specifications to identify changes in critical quality specifications. This includes the choice of dissolution medium, dissolution device and stirring rate. About solid dosage forms of tablets like...