What May Come Of CMS' Proposed Device Regulations

Law360, New York (August 6, 2013, 1:08 PM EDT) -- In its proposed update to the physician fee schedule for calendar year 2014,[1] the Centers for Medicare & Medicaid Services suggested major revisions to its regulations governing Medicare coverage of investigational devices and the routine items and services furnished to beneficiaries during the clinical studies or trials conducted under the U.S. Food and Drug Administration investigational device exemption (IDE) regulations. 

In its proposal, CMS sets forth new standards that would need to be met for the costs of certain investigational devices as well as the costs of routine items and services incurred by...
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