Hall Render

FEBRUARY 14, 2023

The three policy statements include, Department of Justice and FTC Antitrust Enforcement Policy Statements in the Health Care Area (Sept. 15, 1993); Statements of Antitrust Enforcement Policy in Health Care (Aug. Hall Render blog posts and articles are intended for informational purposes only.

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Hospitals Health Care Access Licensing Medicare 45

HIPAA Journal

JULY 15, 2023

HIPAA Guidelines: Seven Elements For Effective Compliance In 2011, HHS published “The Seven Fundamental Elements Of An Effective Compliance Program”. In most cases, the HIPAA Privacy Officer will be the point of contact for members of the public and members of the workforce that want to report privacy concerns.

HIPAA 83

HIPAA Compliance Compliance Officers Licensing 83

New Jersey Healthcare Blog

JANUARY 12, 2022

Exhibits can be reviewed by contacting the New Jersey Individual Health Coverage Program. Exhibits can be reviewed by contacting the New Jersey Small Employer Health Benefits Program. This includes agency name updates, contact information, and addresses. See adopted N.J.A.C. On October 4, 2021, at 53 N.J.R. See adopted N.J.A.C.

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Licensing Medicaid Medicaid Nurses 40

Healthcare IT Today

OCTOBER 18, 2023

Because of the time required to process SDoH, Eye says, institutions need to prioritize which patients to contact. Hands-On Data Collection I talked to Dr. Geoff Rutledge, chief medical officer of HealthTap , a company that came early to telehealth and that I covered several times as far back as 2011.

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Doctors Public Health Medicare Medicare 118

Hall Render

FEBRUARY 15, 2022

In addition, OIG stated that based on the 2019 data the amount of preadmission services at affiliated hospitals was more than 5 times the amount in 2011. Your primary Hall Render contact. Urgent and emergency admissions made up almost 90 percent of admissions associated with outpatient services at affiliated hospitals.

Medicare 40

Medicare Medicare Hospitals Compliance 40

Dot Compliance

OCTOBER 10, 2022

From 2011 to 2015, the top FDA warning letter citation for design controls was design validation. Contact Dot Compliance. Does the device operate in the user’s surroundings? Is the usage of the product simple, unambiguous, apparent, and clear? Is the equipment both patient and user safe and effective?

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FDA Compliance 52

Dot Compliance

OCTOBER 10, 2022

From 2011 to 2015, the top FDA warning letter citation for design controls was design validation. Contact Dot Compliance. Does the device operate in the user’s surroundings? Is the usage of the product simple, unambiguous, apparent, and clear? Is the equipment both patient and user safe and effective?

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FDA Compliance 52

Healthcare Law Blog

SEPTEMBER 28, 2023

Refresher on the RADV Final Rule The Final Rule will implement the following changes: CMS will extrapolate RADV audit findings beginning with payment year (“PY”) 2018, and will not extrapolate RADV audit findings for PYs 2011 through 2017, though it will continue to collect the non-extrapolated overpayments that are identified.

Medicare 52

Medicare Medicare Overpayments Overpayment 52

Health Populi

AUGUST 23, 2021

in July 2021, the lowest read since December 2011. COVID-19 accelerated patients’ expectations of more contact-less payments and online patient financial apps and tools, from scheduling appointments to payment options, plans, and transactions. The University of Michigan’s consumer sentiment index fell to 70.2

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COVID-19 Medical Billing Health Insurance Hospitals 85

Healthcare IT Today

MARCH 25, 2024

Healthcare Has Embraced Mobile Devices According to Pew Research , as of 2023, 97% of Americans own a cellphone and 90% own a smartphone – up from just 35% in 2011. Contact us here or on Twitter at @hcitoday. Siegal to discuss the challenges of managing mobile devices in healthcare. Tell us what you think.

Hospitals 107

Hospitals 107

CMS.gov

APRIL 15, 2019

On March 1 st , we announced enhanced oversight and enforcement of nursing homes that have not improved their antipsychotic medication utilization rates for long-stay nursing home residents since 2011, or “late adopters.” We’ve already reaped rewards from our quality improvement work. percent to a national prevalence of 14.6

Nursing Homes 51

Nursing Homes Nurses Compliance Medicare 51

Hall Render

AUGUST 24, 2023

In this case, the government acknowledged in a 2011 request to extend the seal that its own expert recommended that it intervene in the case. If you have any questions, please contact: Matthew Schappa at (310) 429-3604 or mschappa@hallrender.com ; David Honig at (317) 977-1447 or dhonig@hallrender.com ; or Your primary Hall Render contact.

Governance 40

Governance Due Diligence Hospitals 40

Hall Render

MARCH 24, 2023

The value of the exemption rose 41% from 2011 to 2020 as a result of income growth generated by hospitals during that time period. The $28 billion exemption value exceeded aggregate charity care costs ($16 billion), although nonprofit hospitals also provided community benefits beyond traditional charity care.

Hospitals 40

Hospitals Health Outcomes Nurses 40

Verisys

JULY 13, 2023

Verisys’ former VP of Pharma and Pharmacy Solutions, Joe Thompson, shared a prime example of how speaker programs introduce risk to the pharmaceutical company: “In 2011, one of the most prominent endocrinologists in my sales region was an active speaker for my previous company. He led multiple programs for us each year.

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Compliance Due Diligence Pharmaceutical Industry Fraud 52

Healthcare Law Blog

JANUARY 10, 2022

Please contact Medicare.gov or 1-800-MEDICARE to get information on all of your options.” To ensure MA plan benefits do not discriminate against higher cost enrollees, MA plans are required to establish a limit on beneficiary cost-sharing for Medicare Part A and B services after which the plan pays 100 percent of the service costs.

Medicare 98

Medicare Medicare COVID-19 Medicaid 98

SQA

DECEMBER 10, 2021

This document is a consolidation and revision of IPEC Europe’s GDP Audit Guideline (2011) and IPEC-Americas GDP Audit Guide for North American Distribution of Pharmaceutical Excipients (2011). Devices in direct contact with the central nervous system (CNS), and intended for transient use.

FDA 52

FDA Compliance Public Health Hospitals 52

Health Law Advisor

AUGUST 10, 2023

According to the preamble to the 2011 Final Rule: A purchaser of an MDDS who has only used, configured, or modified the MDDS in accordance with the original manufacturer’s labeling, instructions for use, intended use, original design, and validation would not be considered a manufacturer for purposes of this regulation. 3] 21 U.S.C.

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FDA Licensing Hospitals Medicaid 98

C&M Health Law

JANUARY 25, 2023

For more information, or to better understand how the Act impacts your organization, please contact the professionals listed below, or your regular Crowell & Moring contact. Triggered by enactment of the American Rescue Plan Act of 2021, the 4% cut to the Medicare program would have taken effect in January 2023.

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Medicaid Medicaid Medicare Medicare 104

Hall Render

MARCH 16, 2022

It’s also the first bicameral legislation to include community project funding (previously known as “earmarks”) since they were banned in 2011. Your primary Hall Render contact. Puerto Rico will receive an additional increase of $200 million if HHS certifies that its state Medicaid plan meets certain requirements.

COVID-19 40

COVID-19 Medicare Medicare FDA 40

Drug & Device Law

MARCH 25, 2022

604 (2011), and Mutual Pharmaceutical Co. Various FDA emails and other contacts demonstrated that the FDA issued its complete response letter because the FDA believed that the scientific data were insufficient to support the warning at issue, and was not merely a quibble about the term “stress fracture,” as plaintiffs contended.

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FDA Governance 52

Drug & Device Law

FEBRUARY 25, 2022

We return to a theme we’ve repeated twice before, in 2011 and in 2014 – that in addition to industry-specific groups, manufacturers of prescription medical products should definitely consider joining the Product Liability Advisory Council (“PLAC”). Want more? And PLAC does not do amicus work only.

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FDA 59

Drug & Device Law

SEPTEMBER 26, 2022

2011) (en banc). The MDL lay-low-till-settlement business model involves little if any post-solicitation contact between the attorneys representing the plaintiffs and their ostensible clients. Sec’y of HHS , 654 F.3d 3d 1322, 1340 (Fed. That’s not how the Vaccine Act works. 300aa-10(b).

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Nurses Governance Hospitals 59

Drug & Device Law

NOVEMBER 22, 2022

915 (2011), which added the “at home” limiter to the “continuous and substantial business” standard for general personal jurisdiction. But he’s not a resident of Pennsylvania, and this cause of action had no contact with Pennsylvania. . . . [W]here’s at 46 (referring to “judicial hell holes”). Brown , 564 U.S.

Governance 72

Governance 72

Drug & Device Law

NOVEMBER 27, 2023

Given the nature of both the contacts and the information that was shared, Hawkins decided it was “fair” to preclude the turncoat Dr. Li from testifying. “[G]iven numerous other courts [that] have disqualified Dr.

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Drug & Device Law

JULY 7, 2022

915 (2011), and Daimler AG v. 277 (2014), the court held that registration by itself does not establish sufficient “minimum contacts” with a state because “[a] corporation might qualify to do business in states in which it never undertakes business or establishes a presence beyond appointing a registered agent.” Brown , 564 U.S.

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Drug & Device Law

MARCH 30, 2023

To initiate contact would create a risk of a range of disciplinary actions against the pharmacist. 552 (2011), and especially in the months after the Supreme Court revisited the subject of content-based speech restrictions more generally in City of Austin v. IMS Health, Inc. , Reagan Nat’l Adver. of Austin , 142 S.

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COVID-19 Public Health FDA Governance 75

Drug & Device Law

MARCH 2, 2023

Plaintiffs alleged that they had these contraceptive devices implanted between 2011 and 2013 (presumably in Georgia), and later suffered some combination of a wide range of symptoms that they attributed to “migration” of the device. But BMS and Walden both hold that a plaintiff’s actions cannot qualify as a defendant’s contacts.

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FDA Public Health 59

Drug & Device Law

JANUARY 21, 2024

Dickinson Township , 2011 WL 1577840 (Mag. April 26, 2011), the plaintiffs could not withhold their SS# in an effort to stymie the defendant’s investigation of their medical histories. Fairfield Inn & Suites by Marriott , 2011 WL 6012970, at *2 n.15 1, 2011); Saunders v. Similarly, Breslin v. Accord Archer v.

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