2012, Governance and Licensing - Health Care Compliance Brief

Understanding Climate and Disability Justice: Mitigating Structural Barriers to the Right to Health

Bill of Health

AUGUST 8, 2023

It explains how conditions, forces, and systems, including poverty, discrimination, underlying health disparities, and governance, not only shape daily life but also vulnerability to climate-induced disasters (Figure 1). Source: Jim Evans via Creative Commons License.) Governments are often falling short of this vision.

Governance

Governance Licensing Health Outcomes Nurses

Unlocking the mRNA Platform Technology: Walking the Talk with Investment Protection

Bill of Health

APRIL 7, 2023

By Aparajita Lath Two articles published last month in the BMJ analyze the public investment and financing of mRNA COVID-19 vaccines, highlighting the extensive government funding that has supported the development of mRNA technology from 1985 to 2022. government. government substantially de-risking the vaccine development process.

COVID-19 Vaccine

COVID-19 Vaccine COVID-19 Governance Public Health

Drug Enforcement Administration (DEA) Pulls Controlled Substance Licenses from Two Central Florida CVS Pharmacies

The Health Law Firm

SEPTEMBER 13, 2012

The US Drug Enforcement Administration (DEA) revoked the registrations (controlled substance licenses) from two CVS pharmacies in Sanford, Florida, on September 12, 2012, according to a number of sources. This decision is in response to a government crackdown on the distribution of painkillers.

Licensing

Licensing Governance

Cybersecurity Vulnerabilities in Implantable Medical Devices

HIT Consultant

JULY 11, 2024

Health Sector Cybersecurity Coordination Center and the Office of Information Security, the frequency of healthcare data breaches has trended upward since 2012. Government Accountability Office, each medical device has an average of 6.2 According to a report from the U.S. According to the U.S.

FDA

FDA Hospitals Governance Ransomware

OIG-LEIE, GSA-SAM, and State Medicaid Exclusion Lists: What’s the Difference?

Provider Trust

MARCH 16, 2022

The SAM.gov database is formerly known as the Government Services Administration’s (GSA) list of Excluded Parties List System (EPLS). In 2012, GSA announced it was migrating data from the EPLS to a new and more comprehensive system called the System for Award Management (SAM).

Medicaid

Medicaid Medicaid Medicare Medicare

Password Manager Recommendations for Simpler, Better Security

Total HIPAA

AUGUST 23, 2021

Dashlane has been in business since 2012. Dashlane’s strong security uses AES-256 encryption , which is the same standard used by the federal government to protect classified information. per year plan , where you get five licenses, plus 10GB of secure file storage. Dashlane offers its password manager at $40.00/year

HIPAA

HIPAA Compliance Licensing Governance

How to Increase Your Health Plan’s CMS Star Ratings to Earn More Revenue In 2021

Innovaare Compliance

FEBRUARY 9, 2021

The Affordable Care Act of 2010 mandates the CMS to make quality bonus payments (QBPs) to Medicare Advantage (MA) organizations that achieve at least four stars in a 5-star quality rating system and, starting in 2012, the CMS incentivizes health plans to improve member experiences by increasing the QBP amount, based on their star rating.

Medicare

Medicare Medicare Medicaid Medicaid

What the Law and Bioethics Tell Us About Synthetic Human Embryos

Bill of Health

OCTOBER 13, 2023

There is no specific regulation governing such research in the U.S.; it’s just that the federal government won’t fund the research. This “rejuvenation” of mature cell types was the revolutionary discovery of the Japanese biologist Shinya Yamanaka, which won him a share of the 2012 Nobel Prize in Physiology or Medicine.)

Bioethics

Bioethics Informed Consent Governance Licensing

April-July 2022 State Regulatory Developments

New Jersey Healthcare Blog

JULY 22, 2022

771(a), the Department of Law and Public Safety, Division of Consumer Affairs, State Board of Pharmacy proposed new rules setting forth the requirements to allow a pharmacy to have licensed pharmacists and registered pharmacy technicians perform limited pharmaceutical functions at a location other than on the premises of a pharmacy.

COVID-19 Vaccine

COVID-19 Vaccine Licensing COVID-19 Public Health

Is a Federal Medical License Constitutional?

Bill of Health

JANUARY 3, 2023

Although three in four doctors support scrapping state medical boards in favor of a single federal license, such sweeping reform is likely far off. Some scholars have interpreted this to mean that the federal government has the right under the Commerce Clause to regulate all medical licensure. By Timothy Bonis.

Licensing

Licensing Telemedicine Governance Federal Policy

How the Fifty States View Electronic Data as a “Product”

Drug & Device Law

JULY 31, 2023

Since digital files were not “articles” under the statute, the government could not rely on this statute to prevent their importation. 2012), computer code was not a “product” for purposes of the National Stolen Property Act, 18 U.S.C. 2012 WL 5932437 (N.D. 3d 316, 338 (Alaska 2012). 2012 WL 12886210, at *3 (C.D.

Governance

Governance Payment Systems Hospitals Licensing

NPP, DCC, And FDA-Regulated Medical Products

Drug & Device Law

MAY 26, 2023

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. 452 (2012), which we discussed here but which no NPP opinion mentioned, preemption ruled the day and the DCC never came up.

FDA

FDA Licensing Doctors Governance

Suing the Certifiers – A Dangerous Undertaking

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. Furthermore, trade associations often serve to assist the government in areas that it does not regulate. 2012 WL 3265002, at *5 (N.D. Sizemore v.

Doctors

Doctors Fraud Licensing Compliance

D. Arizona Precludes Pelvic Mesh Punitive Damages

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.”

FDA

FDA Governance Licensing

Health Care Compliance Brief

Understanding Climate and Disability Justice: Mitigating Structural Barriers to the Right to Health

Unlocking the mRNA Platform Technology: Walking the Talk with Investment Protection

Trending Sources

Drug Enforcement Administration (DEA) Pulls Controlled Substance Licenses from Two Central Florida CVS Pharmacies

Cybersecurity Vulnerabilities in Implantable Medical Devices

OIG-LEIE, GSA-SAM, and State Medicaid Exclusion Lists: What’s the Difference?

Password Manager Recommendations for Simpler, Better Security

How to Increase Your Health Plan’s CMS Star Ratings to Earn More Revenue In 2021

What the Law and Bioethics Tell Us About Synthetic Human Embryos

April-July 2022 State Regulatory Developments

Is a Federal Medical License Constitutional?

How the Fifty States View Electronic Data as a “Product”

NPP, DCC, And FDA-Regulated Medical Products

Suing the Certifiers – A Dangerous Undertaking

D. Arizona Precludes Pelvic Mesh Punitive Damages

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