1980, FDA requires IRB review for NSR (non-significant risk) devices1981, FDA and Department of Health and Human Services revise regulations for human subject protection.
Driving Diversity with the Integrated Research Model
October 16th 2024Ashley Moultrie, CCRP, senior director, DEI & community engagement, Javara discusses current trends and challenges with achieving greater diversity in clinical trials, how integrated research organizations are bringing care directly to patients, and more.