Anne Tomalin, Vice President of Quality, Regulatory and Safety will train on the Fundamentals of Regulatory Affairs in Canada providing an overview of getting approval, and maintaining that approval post-NOC, for pharmaceutical products.

This course is relevant for Regulatory personnel who would like a broad overview, or those new to Regulatory Affairs.  Portions of the course would be of interest to New Business Development, Marketing, Quality Assurance or Pharmacovigilance personnel. Medical Devices specific training will be offered in a future course.