Our latest Potpourri captures the excitement of the holidays with scintillating items on certificate of need program effects on utilization, the public's views on health care costs and government's role…
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Everyone is concerned about health spending growth, the primary cause of which is unit price increases. So why are obvious methods to reduce unit price of services, like substituting less-expensive…
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Another brilliant edition of our Potpourri, focusing on individual health insurance rate reform, variation in traumatic care costs, genetic counseling and diabetes, small business and health care costs and savings…
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The New England Journal of Medicine contains an article on the relative review process and outcomes for the FDA, Health Canada, and the European Medicines Agency, with the surprising finding…
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Hospital unit prices appear to be the single largest cause of increased health spending, according to several lines of research. In a new report, the National Institute for Health Care…
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Pay-for-performance programs have enough problems demonstrating that they actually work to improve outcomes and now the Government Accounting Office has identified another potential problem for these initiatives--the federal fraud and…
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Another tremendous edition of our Potpourri, featuring accountable care organization results, waste in our health system, self-referral costs, calculating hospital readmission rates and the benefits, if any, of telemonitoring frail…
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Maryland is unique among the states in having an all-payer hospital rate regulation system. The most recent report on the system's performance shows that it is continuing to constrain the…
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The Food & Drug Administration releases its strategic plan for regulatory science, identifying priority areas and implementation strategies for each. How the FDA carries out its strategy over the next…
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The FDA released a draft guidance on how it will regulate mobile and wireless healthcare devices and applications, which to a large extent follows proposed guidance from the mHealth Regulatory…
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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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