Tue, 10/10/2023 - 12:03
If you’re conducting a clinical investigation of a medical device in a European Union member state, you will be required to submit a clinical investigation report (CIR) along with a summary of the CIR to that member state.
The European Union…Stephanie Hinton
Clinical medical device guru
Stephanie Hinton is a clinical medical device guru with more than a decade of combined experience working in human subjects research. Her expertise includes recruitment strategy, protocol development, IRB submissions and amendments, and preparing for NIH grant applications, as well as coordinating and planning for DSMB meetings.
Tue, 10/10/2023 - 12:03