The FDA's 510(k) medical device approval process has been criticized for requiring too little data on potentially harmful devices. The FDA undertook a review of the process and has issued…
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Our usual end-of-the-week collection of health care tidbits, featuring HIE vendor awards; the point-of-care testing market; what makes medical groups successful; family caregivers and technology; clinical decision software for imaging;…
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Personalized medicine has taken somewhat of a back burner in the wake of reform, but the science continues to evolve. An interesting report looks at how the Department of Defense…
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