Qualification of dissolution instrumentation
- At: 2011 FIP Congress in Hyderabad (India)
- Type: Presentation
- By: BROWN, Cynthia (Eli Lilly & Co, Indianapolis, IN, United States of America)
- Co-author(s): Barker, Amy R. (Eli Lilly & Co, Indianapolis, IN, United States of America)
Deverall, Matthew (Eli Lilly & Co, Indianapolis, IN, United States of America)
Over the last four decades, the dissolution test has evolved into a powerful method for characterizing oral drug products. It is an important tool for assessing lot-to-lot quality of a drug product, guiding development of new formulations and ensuring continued product quality and performance after certain post approval changes. The ability to.. The access to the whole abstract and the presentation file is available to FIP members and to congress participants of that specific congress.