New Jersey Healthcare Blog

JANUARY 12, 2022

This notice extends the waiver of the continuing education requirements for current active health officers and REHSs who are renewing their license for the 2022 licensing period. 10:191, Children’s Partial Care Programs, by the Department in 2007; and N.J.A.C. See N.J.A.C. 8:7-1.11, 1.12, 1.13, 1.17. 10:101 as N.J.A.C.

Licensing 40

Licensing Medicaid Medicaid Nurses 40

Verisys

FEBRUARY 1, 2022

The UPIN Registry was discontinued in 2007 when CMS replaced UPINs with NPI numbers as the preferred provider identification number. In addition to the primary and selected taxonomies, the NPPES search will also return the state code and license number associated with the taxonomy. How Do You Get an NPI Number?

Fraud 52

Fraud Medicare Medicare HIPAA 52

Innovaare Compliance

FEBRUARY 9, 2021

Launched in 2007, star ratings enable the CMS as well as consumers to compare health plans on metrics other than cost. Mismanagement of appeals and grievances can lead to severe penalties, such as lower Medicare star ratings, on the moderate side, while contracts and licenses can be cancelled, at the extreme end of the spectrum.

Medicare 40

Medicare Medicare Medicaid Medicaid 40

Drug & Device Law

JULY 31, 2023

2007 WL 2460776, at *6 (D. 2007 WL 218242, at *4 (N.D. 26, 2007) (bespoke software not a UCC good). 2007), held that “defective computer software may give rise to strict products liability in tort.” Buhimschi , 2007 WL 2902896, at *16 (E.D. 28, 2007), aff’d , 396 F. Henry , 2007 WL 2743097, at *2 (W.D.

Governance 52

Governance Payment Systems Hospitals Licensing 52

Drug & Device Law

MAY 19, 2023

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.

FDA 111

FDA Medical Personnel Telemedicine Licensing 111

Drug & Device Law

JUNE 2, 2022

This was in contrast to state authority to regulate physicians licensed by the state, as in Planned Parenthood of Cincinnati Region v. 124 (2007), which would also be knocked out by Dobbs if it sticks. the state action would be preempted. Strickland , 531 F.3d 3d 406 (6th Cir. Both of these cases applied the U.S. Carhart , 550 U.S.

FDA 127

FDA Licensing 127

Drug & Device Law

MAY 30, 2022

The law presumes that licensed doctors know what they are doing. W]e believe that a drug manufacturer cannot be required legally to foresee that a licensed physician will disregard express warnings regarding a drug’s use. . . . There’s a reason why prescribing physicians and implanting surgeons are called “learned” intermediaries.

Doctors 59

Doctors Licensing Informed Consent Hospitals 59

Drug & Device Law

MARCH 7, 2022

544 (2007), and Ashcroft v. It does not give him license to evade the less rigid ? It does not, however, give a plaintiff “license to evade the less rigid ? The ruling in question was that the TwIqbal ( Bell Atlantic Corp. Twombly , 550 U.S. Iqbal , 556 U.S. though still operative ? strictures of Rule 8. . . . at 570)).

Fraud 59

Fraud FDA Licensing Pharmaceutical Industry 59

Drug & Device Law

AUGUST 8, 2022

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. It verifies that IMGs received a degree from an appropriate institution and administers tests of medical knowledge and English proficiency. 471 (11th Cir.

Doctors 52

Doctors Fraud Licensing Compliance 52

Drug & Device Law

FEBRUARY 20, 2023

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. ,

FDA 59

FDA Licensing Hospitals Governance 59

Drug & Device Law

MAY 26, 2023

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. Prescription drugs are not. And no federal agency specifies an intended use for these products.

FDA 59

FDA Licensing Doctors Governance 59

Drug & Device Law

MARCH 16, 2022

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.” Hence, the statute applied.

FDA 69

FDA Governance Licensing 69

Drug & Device Law

FEBRUARY 2, 2023

2007 WL 4042757, at *3 (N.D. 15, 2007); McNeil v. Texas, unlike most states, enforces a strong statutory presumption that prescription medical product warnings complying with FDA requirements imposed by “pre-market approval or licensing of the product” are adequate as a matter of law. Novartis Pharmaceuticals Corp. ,

FDA 59

FDA Licensing Fraud 59