Submission Evaluation and Post-market Analysis

Course: RGL3300


This course is part of the following part-time on campus and/or online program(s):

The regulatory requirements for a new product continue beyond the regulatory submission, to its evaluation and continued regulatory control once the product is on the market. Students consider the submission approval process and investigate the regulatory concerns for products once they are on the market. Using case studies, students apply the regulatory requirements at various stages in the evaluation of a new drug submission and determine the factors that contribute to approval or rejection.

Notes

This course is part of a graduate certificate program which requires an application process. Web registration is not available. If you have been accepted into the program, please register through the Academic Planner in your ACSIS account. If you would like to apply to this program of study, please complete our free online application form.

Prerequisites

MGT4501

SUMMER 2024
Online Learning
SectionDate(s)ModeDomestic FeesRegistration
800 May 14 - Aug 20Online$461.18* See footnote

Please Note: Off-shore international students enrolling in online courses will be subject to an international premium fee per course registration.


* Online registration not available for this section.

Every attempt is made to ensure the accuracy of the information in this publication. The College reserves the right to modify or cancel any course, program, fee, timetable, or campus location at any time.