Introduction to Regulatory Affairs in Drug Development

When developing new pharmaceuticals, the key to success is to ensure that all regulatory requirements are met throughout every stage of the research and development work.

This course targets an up-to-date overview of current regulation and how to ensure sufficient regulatory documentation in all phases of a drug’s development, with focus on the early phase. The course is primarily aimed at you who work at a small to medium sized research based pharmaceutical company and need an overall knowledge of Regulatory Affairs.

For registration and more information click here.