Regulatory Science Virtual Symposium: “Innovation to Translation: Role of Genomics in Medical Product Development” Session 1: Introduction (2021)


1. Introduction

  • A big welcome to attendees from industry, academia, MPTX classes, etc.!

2. SC CTSI Clinical Research Support (CRS)

  • A comprehensive service aiding investigators and research teams to develop, activate, conduct, and report results for human subject research studies

3. Auditing Module is available now!

  • For access, go to:
  • Created by the USC Department of Regulatory and Quality Sciences
  • To cross train investigators in the practices of monitoring and auditing

4. Georgia CTSA and SC CTSI: Online Course Catalog

5. For more information about the USC Regulatory and Quality Sciences, see the following link:

6. Degree Programs

  • Five Graduate Programs: DRSC, MS Regulatory Science, MS Management for Drug Development, and MS Medical Product Quality
  • Certificates: Food Safety, Regulatory Science, Early Drug Development, Clinical Design and Management, Patient and Product Safety

7. Symposiums

8. Today’s symposium topic

  • Role of genomics in medical product development

9. Agenda

10. Program Evaluation

  • Please complete the evaluation at the end of the symposium to receive your certificate.


Accompanying text created by Annie Ly | Graduate Student, Regulatory Science, USC School of Pharmacy and Emily Donahue | Undergraduate Student, Pharmacology and Drug Development, USC School of Pharmacy


Eunjoo Pacifici, PharmD, PhD
Chair and Associate Professor of Regulatory and Quality Sciences Associate Director, D. K. Kim International Center for Regulatory Science

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.