HHS ADDING TECH REQUIREMENTS — HHS is proposing to add standards to its contracts for health information technology. In a proposed rule released Thursday, HHS said that health IT procured by or for HHS, or procured through contracts with providers and insurers that involve implementing or upgrading health IT, must meet certain standards related to data exchange. The agency said that doing so offers clear guidelines for health tech and can reduce burden for developers, while making it easier to share data across systems. The agency is taking comments from the public for 60 days after the proposal is published in the Federal Register. The reaction: Health IT advocacy group the Health Innovation Alliance hammered the proposal, saying “everyone should be concerned.” “Historically, the government does not do technology well, yet we’re seeing government reach far and wide to control and dictate technology used in health care,” the group said in a statement. DEVICE MAKERS TO CMS: DO MORE — CMS’ new rules offering broader coverage from some medical devices is drawing lackluster reviews from the medical device industry. The details: The Biden administration in 2021 overturned a policy, enacted during President Donald Trump’s administration, that allowed four years of Medicare coverage to FDA-approved breakthrough devices, saying it went too far. On Wednesday, CMS finalized a proposal narrower than the Trump proposal allowing devices to be covered on a transitional basis that are relevant to the Medicare population. The agency said it expects to accept up to five candidates a year for Transitional Coverage for Emerging Technologies. The reaction: Scott Whitaker, CEO of trade group AdvaMed, said in a statement the move is a "step toward a stronger, more robust policy" but isn't sufficient. “The limited number of devices CMS can handle demonstrates clearly to Congress the need for greater resources at CMS,” said Whitaker, who called for lawmakers to pass bipartisan legislation mandating Medicare cover FDA-approved breakthrough devices for four years. Mark Leahey, CEO of the Medical Device Manufacturers Association, also backed the bill and said the trade group is “disappointed” by the move. Leahey said that limiting coverage to five candidates a year won’t “meaningfully improve access or address disincentives to medical innovation.” HALTING CAT RESEARCH — Medical testing on cats has come to an end at the Department of Veterans Affairs, an agency spokesperson confirmed to Pulse. According to web archives, the agency as recently as April had planned research involving prosthetics on felines. “VA has conducted research using sensitive species when absolutely necessary to care for those who have served in our military,” agency spokesperson Terrence Hayes said. “Under Secretary [Denis] McDonough, this practice has begun to come to an end.” The move comes after Congress in a spending bill this year barred VA animal testing within two years, with some exceptions. Hayes said the VA is “fully complying.” The agency has approved research involving canines and non-human primates. Congress’ decision came after pressure from groups like the White Coat Waste Project, a watchdog group that opposes federally funded animal experiments.
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