What is their Role in Cancer Research and Development?
In cancer research and development, regulatory affairs professionals are involved in every stage from preclinical research to post-market surveillance. They are responsible for compiling and submitting regulatory submissions such as Investigational New Drug (IND) applications and New Drug Applications (NDA) to agencies like the FDA and the EMA. Their work ensures that all data is compliant with regulatory standards and that the benefits of the new therapies outweigh the risks.
