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
| WINTER 2025 |
| Online Learning |
| Section | Date(s) | Mode | Domestic Fees | Registration |
|---|---|---|---|---|
| 800 | Jan 14 - Apr 22 | Online | $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 is 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.