Biotech product development for major markets such as US/EU as well as other regions of the world is continuing to increase. Analysis shows that developers who prepare global upfront strategies and utilize risk-based tools benefit from efficiency and save resources leading to faster market entry. This talk provides an overview of biotech drug development and focusses in the most common CMC pitfalls we have recently observed and how to avoid them.
Key learning objectives:
- Updated overview of the multidisciplinary (CMC, non-clinical and clinical) requirements for the development of biotech products
- Outline of the recent regulations, highlights critical requirements
- Summary of the most common CMC pitfalls we have recently observed and how to avoid them
