“Principles of Global Clinical Research for Medical Devices” - Regulatory Science Symposium - Session 6: Wrap-Up (2021)

Regulatory & Quality Sciences
“Principles of Global Clinical Research for Medical Devices” - Regulatory Science Symposium - Session 6: Wrap-Up (2021)
Eunjoo Pacifici, PharmD, PhD

Director of Regulatory Science Services

Course Syllabus/Topics

1. Please complete program evaluation survey to receive your certificate
2. Wrap-up discussion

Acknowledgement

Accompanying text created by Annie Ly | Graduate Student, Regulatory Science, USC School of Pharmacy lyannie@usc.edu

Video Series

“Principles of Global Clinical Research for Medical Devices” - Regulatory Science Symposium - Session 6: Wrap-Up (2021) View Video Series
Back to Library >

NIH Funding Acknowledgment: Important - All publications resulting from the utilization of SC CTSI resources are required to credit the SC CTSI grant by including the NIH funding acknowledgment and must comply with the NIH Public Access Policy.

This program is open to all eligible individuals. SC CTSI operates all of its programs and activities consistent with the University’s Notice of Non-Discrimination. Eligibility is not determined based on race, sex, ethnicity, sexual orientation, or any other prohibited factor.

For our complete Terms of Use, including privacy and legal compliance statements, click HERE.  Copyright © 2026 SC CTSI: Southern California Clinical and Translational Science Institute at USC and CHLA. All rights reserved.