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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