Forced Degradation for Pharmaceuticals 2015 is a conference that covers topics such as:
- Sharing experiences of successful stress testing conditions and limits
- Comparing and practically complying with regulatory requirements for forced degradation studies in Europe, USA and Japan
- Best practices for conducting photolytic degradation studies
- Practically carrying out oxidative degradation studies
- Generics perspective: Practically designing and implementing forced degradation studies
- Accurately predicting drug product and drug substance shelf-life through science-based accelerated degradation studies
- Practically applying genotoxic impurity guidelines to forced degradation studies, including ICH M7
- Forced degradation and stability studies – from small to large - similarities and differences
- Successfully implementing excipient compatibility studies and understanding the impacts of excipients on degradation pathways to optimise formulation development
- Practically implementing forced degradation studies for drug product development
- Practically applying QbD to forced degradation studies
Forced Degradation for Pharmaceuticals 2015 brings together attendees involved in:
- Development
- Analytical
- Formulation
- Stability
- Chemistry
- R&D
