Regulatory Affairs Generic Drugs
The objective of this course is to provide students with overview and background of the Generic drugs. The product development process, regulatory requirements and various differences of the generic drugs vs. novel drugs are discussed in details. The course also covers in depth discussion of international food and drug laws, regulations and guidelines for the registration of Generic drugs.
This course is intended primarily for students wishing to pursue a career in the pharmaceutical industry, in Regulatory Affairs Departments.
In Class Registration CAD$300 +HST | Online Education Registration CAD$200 +HST