Regulatory Affairs for Medical Devices
This course will introduce students to the field of medical devices that are not falling under the category of drugs and will define medical devices, discuss existing challenges for innovative research, medical devices classification, international and local guidelines and regulations regarding the devices’ approval and the conduct of associated clinical studies required for regulatory approval. In addition, the course will outline clinical research involving medical devices and regulations for medical devices‘ safety monitoring and safety reporting.
This course is intended primarily for students wishing to pursue a career in the pharmaceutical industry, in Clinical Research, Drug Safety, and Pharmacovigilance.
In Class Registration CAD$720 +HST | Online Education Registration CAD$450 +HST