Dissolution is a critical parameter of pharmaceutical dosage forms. It is well recognised that in-vitro dissolution testing is relied upon to screen formulations during development and to ensure batch-to-batch quality control during routine release testing. Dissolution is the process by which a solid solute enters into solution in the presence of solvent. Dissolution rate may be defined as the amount of active ingredient in a solid dosage form dissolved in unit time under standardised conditions of liquid/solid interface, temperature and media composition. We have invested in state-of-the-art dissolution apparatus that meets the requirements of international regulations. Together with our extensive experience in developing, validating and executing dissolution test methods, for various applications and across a variety of product types, we are confident that we can meet your expectations.