How to Submit a Grant Application and Activate Clinical Studies at USC
In this video, you will learn about the process of submitting a grant application at USC, and the various offices involved throughout the process. In addition, you will learn about what to do after your grant is funded, and how to go about activating and…
Regulatory Science Symposium: Clinical Trials with Medical Devices Session 9: Wrap Up (2019)
In this series, we will discuss considerations, regulations and resources to utilize when conducting clinical trials with medical devices.
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 Science Symposium: Clinical Trials with Medical Devices Session 7: Auditing of Medical Device Trials (2019)
In this series, we will discuss considerations, regulations and resources to utilize when conducting clinical trials with medical devices.
Regulatory Science Symposium: Clinical Trials with Medical Devices Session 6: Advanced International Trials with Medical Devices (2019)
In this series, we will discuss considerations, regulations and resources to utilize when conducting clinical trials with medical devices.
Regulatory Science Symposium: Clinical Trials with Medical Devices Session 5: Medical Device Feasibility Clinical Trials – SetPoint Medical Case Study (2019)
In this series, we will discuss considerations, regulations and resources to utilize when conducting clinical trials with medical devices.
Regulatory Science Symposium: Clinical Trials with Medical Devices Session 4: Quality at the Data Level (2019)
In this series, we will discuss considerations, regulations and resources to utilize when conducting clinical trials with medical devices.
Regulatory Science Symposium: Clinical Trials with Medical Devices Session 3: IRB Reviews on Medical Device Trials (2019)
In this series, we will discuss considerations, regulations and resources to utilize when conducting clinical trials with medical devices.