FDA plans to conduct a cognitive study of health care practitioners this summer to advance efforts to standardize the structure and content of medical device labeling. While the device industry is providing advisory assistance for the project, sector advocates remain skeptical that broad-scale standardization for device labeling is feasible or advisable.
Researchers working with CDRH will visit several hospitals in the Washington, D.C., area and also bring clinicians to the agency’s Silver Spring, Md