Dissolution testing for pharmaceutical products has significant role in drug development and is used in all phases of development for quality control testing to assess batch-to-batch consistency, product release and stability testing programs.
It is key analytical test used for detecting physical changes in an active pharmaceutical ingredient (API) and in the formulated product.
Our dissolution study services include:
Dissolution profile studies carried out according to USP (711〉, EP, BP and/or customer requirements
Development and validation of dissolution studies (Release/Discriminatory)
