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government for false or fraudulent claims submitted for federal reimbursement. Because FCA relators pursue the governments claims, several circuits have determined this precludes relators from proceeding pro se. The government declined to intervene and, in a filing with the U.S. Background The FCA, codified at 31 U.S.C.
The 24 defendants, among them CEOs associated with five telemedicine companies, the owners of dozens of DME companies and three licensed medical professionals, allegedly participated in healthcare fraud schemes involving more than $1.2 billion in losses. ON THE RECORD.
NPIs are critical for maintaining accountability across healthcare transactions, ensuring accurate reporting, and streamlining electronic communication across private and government health insurance programs. The state license number linked to the taxonomy is also displayed.
Launched in 2007, star ratings enable the CMS as well as consumers to compare health plans on metrics other than cost. The higher the ratings, the larger the bonus payments health plans receive from the government. The CMS star ratings challenge. With billions of dollars at stake for payers with CMS star ratings above 3.5,
Inside one of the most-fined nursing homes in Mass But if the federal government wont require minimum staffing standards, states can. If the federal government returns to the toothless per instance fines for inadequate care adopted by the first Trump Administration, states can impose their own, meatier penalties. Some already do.
Since digital files were not “articles” under the statute, the government could not rely on this statute to prevent their importation. 2007 WL 2460776, at *6 (D. 2007 WL 218242, at *4 (N.D. 26, 2007) (bespoke software not a UCC good). at 1291-93 (construing 19 U.S.C. at 1291-92. at 1293-94. Similarly, in United States v.
Both talk a fair amount about “commerce” and the respective roles of the states and federal government. You never need an authorization from a licensed professional to buy pork or fireworks. One of those laws, FDAAA in 2007, established the REMS system, which reflects the importance of national uniformity in the delivery of healthcare.
at *1, by threatening to revoke the license, and jail for at least three years, any West Virginia physician so bold as to prescribe the plaintiff’s FDA-approved drug for its FDA-approved use. Sorsaia , 2023 WL 3211847, at *7 (citations omitted). See also GenBioPro, Inc. Sorsaia , C.A. 2023 WL 3451688, at *1 (S.D.W.
Without an FDA license to produce another design, [defendant] was legally prohibited from distributing either [alternative design advocated by plaintiffs] at the time [plaintiff] received her vaccinations. As a result, appellee was prohibited by federal law from employing either of these [alternatives]. Wyeth Laboratories, Inc. ,
For qualified IMGs, it issues a certification, which IMGs can then use to apply to residency and other graduate medical education programs and to apply for state medical licenses. Furthermore, trade associations often serve to assist the government in areas that it does not regulate. at 183 (quoting Meyers v. Donnatacci , 531 A.2d
In Arizona, a manufacturer cannot be liable for punitive damages if the product was “designed, manufactured, packaged, labeled, sold or represented in relevant and material respects according to the terms of an approval, conditional approval, clearance, license or similar determination of a government agency.”
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