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FDA’s own documents reveal agency’s lax, slow, and secretive oversight of clinical research

External Link - Source: Science

When considering clinical research and oversight, who is in charge? The FDA is the main agency that deals with clinical oversight, but from research, “FDA’s enforcement of clinical research regulations is often light-handed, slow-moving, and secretive.” How does this relate with current clinical trials of COVID-19? How can we ensure that certain researchers are being watched for their clinical research practices?