Regulatory Science Symposium: "Ensuring Clinical Trial Compliance" Session 7 - Wrap-up

Regulatory & Quality Sciences
Study & Site Management
Research & Study Conduct
Regulatory Science Symposium: "Ensuring Clinical Trial Compliance" Session 7 - Wrap-up
Eunjoo Pacifici, PharmD, PhD

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

Competencies: Audits, Pharmacy, Regulatory Science, Clinical Research and Regulations, Project Management, Clinical Trials, Regulatory and Quality Sciences, Clinical Trial Quality

Course Syllabus/Topics:

  • Resource: Ensuring Clinical Trial Compliance
    • Can be found in the electronic binder
  • Complete program evaluation survey to receive certificate of completion
  • Poll Time!
  • Thank you!


Acknowledgements:
Accompanying text created by: Roxy Terteryan, Project Administrator, SC CTSI
Rushaanaaz Sokeechand, Student Worker; Mahita Parasa, Student Worker

Video

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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.