Stability testing and evaluation of pharmaceutical products are required to determine the changes in the quality of a drug substance over time. Regulators want to know the shelf-life of your product by examining how it behaves in various environmental factors such as temperature, humidity and light.
This training course examines all aspects of stability testing and evaluation of small molecules pharmaceuticals. Topics covered include protocol design Q1A, validation, forced degradation studies, stability evaluation ICH Q1E, reduced study designs, climatic zones ICH Q1 F and photostability studies ICH Q1B.
With the Educo Post Learning Implementation Plan (PLIP) you will have the framework to apply and implement the knowledge acquired in the training, supporting you in your development. Learn more about how we deliver online and classroom training.