Flyer "Dissolution Rate Testing" download ›
An essential part of the quality control of solid dosage forms is to determine the dissolution rate. The pharmacopoeias describes different apparatuses, suitable for different tasks (Ph. Eur. 2.9.3 and USP ICH harmonized in Q4B Annex 7R2 and Ph. Eur. 9.2.42, 2.9.43 and ). Due to the high number of devices, continuous qualification work and the great experience ensure that both, time-critical analysis e.g. batch release testing as well as problem solving can be performed.