Introduction to Dissolution Method Development & Validation 2016 is a webinar that covers topics such as:
- Strategies for selecting dissolution conditions, including medium, apparatus and time points
- Several different reasons for developing dissolution methods, and corresponding differences in the approaches
- Trending of results and change control
- Why dissolution method validation is more complex than that for other methods
- Pointers for proposing specifications
Introduction to Dissolution Method Development & Validation 2016 is intended for attendees from:
- Formulators who rely on dissolution data and regulatory affairs/CMC personnel responsible for filings involving dissolution
- Chemists (Research, Quality Control, and CRO; Human, Veterinary or Generic) involved with dissolution method development or testing and their managers