During this workshop all relevant aspects regarding the quality assessment of post approval changes in pharmaceuticals will be discussed. You will get to know:
- Understanding the requirements of minor and major variations.
- Learn about some commonly encountered deficiencies and how to address them.
- The current guidance and risk assessment for nitrosamine impurities.
14-12-2022 11:00:00 am
14-12-2022 2:00:00 pm