ISCI 353

Regulatory Affairs

University of South Dakota · UGRD · Fall 2026

1 section

Catalog description

In this course students will become acquainted with US regulations for medical devices and pharmaceutical products including device classification, 510(k) notification and the pre-market approval process. Prerequisites and Corequisites Prerequisites: ISCI 215 - Good Laboratory Practices / ISCI 215L - Good Laboratory Practices Lab

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Class #south_dakota_2-ISCI353Fall 2026UGRD3 credits

Days & times: No scheduled meeting time
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Instructor: Staff

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