Regulatory Science Symposium: “Innovations in Regenerative Medicine Products” - Session 1: Introduction

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

Syllabus/Topics

  1. Introduction
    1. A big welcome to onsite students from regulatory and quality sciences classes, and online guests from industry, academia, USC Alpha Clinic/California Institute for Regenerative Medicine (CIRM) community, etc.!
  2. SC CTSI Clinical Research Support (CRS)
    1. A comprehensive service aiding investigators and research teams to develop, activate, conduct, and report results for human subject research studies.
  3. Clinical Trial Quality Training Series
    1. Free e-learning modules available for public use

Created by the USC Department of Regulatory and Quality Sciences and Regulatory and Knowledge Support (RKS) core within SC CTSI

For access, go to: https://uscregsci.remote-learner.net

  1. Georgia CTSA and SC CTSI: Online Course Catalog
    1. Offers free training for clinical research workforce to the first 400 registrants
    2. Provides unlimited courses
    3. Contact hours (CE credits) can be used for CRP certification renewal
    4. Link: https://twd.ce.emorynursingexperience.com/
  2. Regulatory Science Web Portal – coming soon
    1. One-stop shop of regulatory resources with pre-consultation information for investigators
    2. Intended to streamline translation of Investigator-initiated Trials to treatment
  3. For more information about the Department of Regulatory and Quality Sciences at USC Alfred E. Mann School of Pharmacy and Pharmaceutical Sciences, visit our website: http://regulatory.usc.edu
  4. Degree Programs
    1. Five Graduate Programs: DRSC, MS Regulatory Science, MS Management for Drug Development, and MS Medical Product Quality

Launching new graduate program, MS in Clinical Trial Management

  1. Certificates: Food Safety, Regulatory Science, Early Drug Development, Clinical Design and Management, Patient and Product Safety


A
cknowledgment
Accompanying text created by Roxy Terteryan, RKS Project Administrator, SC CTSI (atertery@usc.edu)

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.