Forced Degradation for Pharmaceuticals 2013 is a conference that covers topics such as:
- Real life industry case study: Practically complying with regulatory requirements for forced degradation studies
- Critical overview of regulatory requirements and expectations for forced degradation studies in chemicals
- Case examples of specific products: Stress tests to assess stability differences among the different physical forms of an active substance
- Real life industry case study: Stress testing conditions and limits
- Practical advice for carrying out hydrolytic degradation studies
- ROUND TABLE DISCUSSION: Understanding when is the right time to perform a forced degradation study during development
- Accurately predicting shelf life through science-based degradation studies
- Evaluating the key similarities and differences in stability studies for large and small molecules
- Real ife industry case study: Strategies for identifying and potentially genotoxic degradants
- Practically applying genotoxic impurity guidelines to forced degradation studies
- Conducting forced degradation studies on potential new drug candidates as part of transition from discovery to development
- In silico prediction of forced degradation and interactions with excipients
- Real life industry case study: Practically applying the optimum separation and analysis techniques during forced degradation studies
Forced Degradation for Pharmaceuticals 2013 brings together Directors, Heads of Department, Researchers, Managers and Scientists involved in Analytical chemistry, Analytical sciences, Organic chemistry, Degradation chemistry, Development analysis, Structural analysis, Formulation and Stability.
