Regulatory Science Symposium: Clinical Trials with Medical Devices Session 8: Gaps and Opportunities in Pediatric Device Trials (2019)

In this series, we will discuss considerations, regulations and resources to utilize when conducting clinical trials with medical devices.

Regulatory & Quality Sciences
Study & Site Management
Research & Study Conduct

Topics

  1. Pediatric Medical Devices – an Underserved Area
  2. Pediatric Medical Devices – Overcoming Disparities
  3. Consortium Institutions
  4. Local Ecosystem
  5. The West Coast Consortium for Technology and Innovation in Pediatrics (CTIP) Team
  6. How CTIP supports Medical Device Innovation
  7. Regulatory Considerations for Pediatric Medical Devices
  8. FDA Medical Device Classification
  9. Regulatory Considerations for Pediatric Medical Devices
  10. Takeaways

Acknowledgement

Accompanying text created by Khyati Ashtekar | Graduate Student, Regulatory Science, USC School of Pharmacy | ashtekar@usc.edu

Video Series

Regulatory Science Symposium: Clinical Trials with Medical Devices Session 8: Gaps and Opportunities in Pediatric Device Trials (2019) View Video Series
View More Courses >

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.