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

Regulatory & Quality Sciences
Eunjoo Pacifici, PharmD, PhD

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

Topics

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: https://uscregsci.remotelearner.net
  • 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: http://regulatory.usc.edu

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.

Acknowledgement

Accompanying text created by Annie Ly | Graduate Student, Regulatory Science, USC School of Pharmacy lyannie@usc.edu and Emily Donahue | Undergraduate Student, Pharmacology and Drug Development, USC School of Pharmacy emilydon@usc.edu