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The move to electronic medical records may be helping identity thieves.
Five state legislatures now allow terminal patients to circumvent the FDA. Will this new path to experimental drugs help or hurt?
New digital systems can help keep infectious agents at arm’s length—or further away.
For patients to be effective partners in their own care requires a basic grasp of medical terms that, shockingly, many don’t have.
Lucian Leape, the father of the modern patient safety movement, talks about the culture of disrespect in medicine—and how to fix it.
A prototype program aims to improve adverse event reporting by giving patients, family members and others a voice in the conversation.
Physicians routinely prescribe drugs for uses not approved by the FDA. But should drug reps be allowed to tout those uses?
May problems with therapies show up post-FDA approval. Could mining electronic data and online chatter head off trouble?
In 1966, the anaesthetist-in-chief of Massachusetts General Hospital published a paper that would yield greater protection for clinical trial subjects.
It’s much easier to get a medical device approved than to bring a new drug to market. Should that change?
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