Recently I participated in a discussion on a LinkedIn forum (Quality by Design or QbD) explaining relevance and critical importance of drug dissolution testing for QbD, manufacturing of the products (tablet/capsules) and their evaluations.
Continuing on the topic, I believe a better organized explanation may be useful in clarifying issues related to the assessment of quality of pharmaceutical products. This article provides the explanation. It is important to note that the following discussion is restricted to tablet and capsule products only. Please click here for complete article
