SMPD 283A

Regulatory Affairs I

Description
Provide foundational knowledge of the pharmaceutical, biotechnology and biodevice industries with focus on company organization, product development and commercialization-associated activities such as chemical synthesis, device prototyping, quality assurance, regulatory affairs, manufacturing, control, marketing, and post-marketing surveillance. Prerequisite: Admission to the MPDM program.

Grading
Normal Grade Rules

Units
3