Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices — Toronto

Submitted by neuglobal on Fri, 08/12/2016 - 18:10
Master's in Medical Regulatory Affairs
Major
Regulatory Affairs
Program Description

The Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices program is designed to produce graduates who are highly qualified to manage the regulatory process for companies innovating and developing cutting-edge products in science and medicine.

Curriculums
Title Status Year
Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices (mktg) publish 2020
Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices (mktg) publish 2019
Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices archive 2019
Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices - Marketing archive 2019
Master of Science in Regulatory Affairs for Drugs, Biologics, and Medical Devices publish 2018
MS Regul Aff/Drugs/Biol (CPS) archive 2017
MS Regul Aff/Drugs/Biol (CPS) archive 2018
Location
Toronto
Commitment
Full-Time
Part-Time