Class Number: 2420
Description: Hours: Three hours lecture per week Prerequisite: Admission to the Biotechnology & Bioinformatics, M.S. or the Biotechnology, M.S. & M.B.A. Dual Degree program Description: An introduction to the foundational knowledge and skills necessary to successfully conduct clinical trials for new drugs, biologics, and medical devices, including in vitro diagnostics. Topics include a broad overview of the product development process in the pharmaceutical, biopharmaceutical, and medical device industries, the regulatory and operational requirements for clinical study setup and management, monitoring, data management, and closure of clinical trials, the principles of Good Clinical Practice (GCP), and the applications of quality control and quality assurance. The integration of quality assurance throughout the medical product development process will be discussed.

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Days Time Date Range Location Instructor
W 06:00 PM - 09:00 PM 01/20/2024 - 05/17/2024 Sierra Hall 1422 Timothy Osslund
Status: Open
Session: Extended Session 1
Units: 3.00
Class Components: Lecture
Career: Postbaccalaureate
Start Date: 01/20/2024
End Date: 05/17/2024
Grading: Letter Grade

Class Availability

Information below is 24 hours old.
Enrollment Total: 25
Available Seats: 5
Wait List Capacity: 5
Wait List Total: 0


Enrollment Information

  • Graduate Division
  • In-Person
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