Clinical trial data "one-stop shopping" public registry proposed by Sens. Feinstein, Snowe.
This article was originally published in The Gray Sheet
CLINICAL TRIAL DATA "ONE-STOP SHOPPING" PUBLIC REGISTRY for people with serious or life-threatening diseases will boost participation in clinical research, Sen. Diane Feinstein (D-Calif.) said Aug. 2 in introducing a bill (S 2024) to create such a registry. "With a national database enabling people to find research trials, more people could be available to participate in research. This can help researchers broaden their pool of research participants," Feinstein said. The bill is co-sponsored by Sen. Olympia Snowe (R-Maine).
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