|
Apr 19, 2024
|
|
|
|
CLRA 583 - Regulatory Affairs in Drug Development III This course is part of a 3-course sequence that provides a working knowledge of pharmaceutical regulatory affairs. Emphasis is on a US development, although topics will include non-US development and the development of biologics, OTC and devices. This course addresses post-approval issues including advertising and promotion, drug safety and pricing.
Credit Hours: 3 hrs Grade Mode: Normal (A-F)
Typically offered Fall
Prerequisite(s): and
Last Updated: Course Rotation 9/2014, 07/2011; May 2011
Summer 2024 Course Sections
Fall 2024 Course Sections
Add to Portfolio (opens a new window)
|
|