Annals of Family Medicine

NOVEMBER 20, 2024

These included people with lived/living experience of drug use, clinicians, researchers, government health department staff, and individuals from non-government organizations focusing on drug use. specialists, social workers), thus providing care continuity. specialists, social workers), thus providing care continuity.

Primary Care 130

Primary Care Chronic Disease Management Chronic Disease Government 130

Physician's Weekly

JUNE 19, 2025

Had she signed up for the government insurance plan when she turned 65, Diamond could have avoided a financially perilous situation that left her unexpectedly responsible for the medical costs she incurred during that time. Some of those providers are now seeking payment from her. The bills totaled more than $100,000.

Insurance 52

Insurance Patient-Centered Government Provider 52

Physician's Weekly

JUNE 26, 2025

When a child has risk factors but has not developed the disease, we must continue to provide preventive care and support for the family and appropriately match intensity and dose of the intervention. What modifications would you recommend to clinicians? This starts with recognition that obesity is a chronic disease.

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California Academy of Family Physicians (CAFP)

MAY 14, 2025

Key Health Care Budget Proposals: Proposed Medi-Cal Cuts and Enrollment Changes Medi-Cal, California’s Medicaid program, is typically funded through a partnership between the state and the federal government. To fill that gap, California has chosen to use state-only funds to provide certain Medi-Cal benefits to undocumented Californians.

Healthcare 130

Healthcare Family Physician Management Individual 130

FDA Law Blog

DECEMBER 4, 2023

Houck — Separate decisions by federal district courts in Texas and Puerto Rico in the past two months provide cautionary tales for every pharmacy and wholesale distributor dispensing or distributing controlled substances. The government asserted additional allegations that are outside our scope. 11, 2023 ( DOJ Press Release ).

Treatment Plan 139

Treatment Plan ER Government Patient-Centered 139

FDA Law Blog

SEPTEMBER 28, 2021

Richardson — On September 24, 2021, the owner of a pharmacy in Puerto Rico pleaded guilty to participating in a felony conspiracy to convert government property and to commit health care fraud in connection with the illegal vaccination of minors between the ages of 7 to 11 with the Pfizer-BioNTech COVID-19 vaccine. By Kalie E.

Vaccination 98

Vaccination Individual Government Provider 98

Minnesota Academy of Family Physicians

MARCH 27, 2025

As we move into the tenth week of the legislative session, Minnesota Academy of Family Physicians (MAFP) lobbyist Megan Verdeja breaks down what’s happening at the Minnesota State Capitol and provides an update on health care bills. The bill passed by a voice vote and was referred to the State and Local Government Committee.

Family Physician 52

Family Physician Insurance Finance Individual 52

FDA Law Blog

AUGUST 26, 2021

To hold a corporation liable for these actions, the government must establish that the corporate agent’s actions (i) were within the scope of his duties and (ii) were intended, at least in part, to benefit the corporation. In light of the above, the government generally resists the notion that an organization is a victim of its own employees.

Government 98

Government Manufacturing Individual IT 98

My Green Doctor

APRIL 4, 2025

The Power of Healthcare Professionals as Trusted Messengers Patients Trust Their Healthcare Providers A recent study found that 64% of physicians recognize environmental sustainability affects their patients’ health, yet only 17% feel comfortable discussing it ( PubMed ). The healthcare sector contributes 8.5% of total U.S.

Healthcare Professional 52

Healthcare Professional Healthcare Community Medical Advice 52

BMJ

AUGUST 20, 2021

Donors, government ministries, agencies and academic partners regularly cascade requests for data that multiply and complicate the simple interaction into a complex, and often redundant, set of data requirements for the same singular interaction. Mobile phone penetration has finally exceeded 90% in low- and middle-income countries.

Patient-Centered 40

Patient-Centered Clinic Provider Patients 40

ABIM

APRIL 24, 2025

Dave, MD, MPH , inquired how stressors may contribute to candidates failing the certification examination and Dr. McDonald stated that knowledge gaps were the primary cause, though ABIM provides safeguards to reduce stress like grace periods and consideration of compassionate exemptions for extraordinary life circumstances.

Board-Certified 40

Board-Certified Board-Certified Physicians Community Government 40

Permanente Medicine

MAY 20, 2025

” “Whether you’re the call center agent, the receptionist, [or] the lab tech, you participate and you provide the input into innovation,” said Dr. Nguyen. The Southern California Permanente Medical Group is one of the largest medical groups in the nation with more than 8,800 physicians providing care for over 4.8

Patient-Centered 52

Patient-Centered Patients IT Medical 52

FDA Law Blog

MAY 19, 2025

For a controlled substance prescription to be effective, that is valid, it must be issued for a legitimate medical purpose by an individual practitioner acting in the usual course of their professional practice. By Larry K. Houck Last month the U.S. Attorneys Office, Northern District of Illinois, April 21, 2025. 81, 86, 251. 81, 89, 251.

Individual 64

Individual Patients Provider Medical 64

The Clinical Problem Solvers

NOVEMBER 22, 2021

Together, these two phenomenal guests help us understand the structural and individual challenges of Indigenous peoples in academic medicine, public health, and beyond. It notably creates a burden of proof for Indigenous trainees to prove their identity, which can provide additional stress during application and interview cycles.

Community 52

Community Patient-Centered Medical Student Medical 52

My Green Doctor

MAY 3, 2025

For instance, the UK government’s initiative to install solar panels on National Health Service sites is projected to save each site up to £45,000 annually, amounting to approximately £13 million in total savings per year. The breadth of services provided by modern day medicine is profound. The use of medications in U.S.

Healthcare 52

Healthcare Healthcare Professional Consulting Management 52

FDA Law Blog

APRIL 10, 2025

federal law enacted in 1967 to promote transparency and accountability in the federal government by granting the public the right to request access to government records, subject to certain exemptions. FOIA is a U.S. In some cases, previously routine postings are delayed or going unpublished altogether.

Government 59

Government Provider Community Individual 59

BMJ

JULY 17, 2020

A multilayered view of stigmatizing discourses lays the foundation for eliciting a series of suggestions for quelling stigma, to be implemented at the individual, community, and national levels, as suggested by the WHO. Ebola-related stigma in Ghana: Individual and community level determinants. Scholars such as Wen et al.

Community 40

Community Individual Physicals Finance 40

GeriPal

JULY 19, 2024

What should we use to screen individuals? Joe 03:55 You know, my thoughts are screening is important for a variety of reasons, and certainly Doctor Boris and Soo and Anna, Doctor chodos can provide a lot greater clinical insight than I. Should it? If so, how do we screen and who do we screen? Who should get it if anyone?

Screening 120

Screening Primary Care Patient-Centered IT 120

FDA Law Blog

MAY 7, 2025

Two recent cases from the Fifth and Seventh Circuits, however, support the legality of these arrangements in the absence of the government proving certain circumstances. Sorenson follows the Fifth Circuits decision last year in United States v. Marchetti, 96 F.4th Marchetti, 96 F.4th Medicare or Medicaid).

Referral 59

Referral Relationship Government Healthcare 59

33 Charts

OCTOBER 2, 2021

Inconsistency in care delivery So as every provider shapes her practice around MyChart, each will do it in a slightly different way. And individual practice styles are fine. But this may not be consistently applied by other providers in the same group. Crucial that we fix this. The problem comes with call and cross-coverage.

Patients 75

Patients IT Provider Family Doctor 75

FDA Law Blog

OCTOBER 13, 2024

Designed to incentivize the development of drugs for pediatric rare diseases where such development may not otherwise have occurred, vouchers may be granted for drugs for serious or life-threatening rare diseases where the serious or life-threatening manifestations primarily affect individuals aged from birth to 18 years.

Government 64

Government IT Education Individual 64

FDA Law Blog

NOVEMBER 6, 2022

Now, after an unfavorable HHS Office of the Inspector General (OIG) advisory opinion and two defeats in court, Pfizer has appealed the Second Circuit’s decision to the Supreme Court. At the center of Pfizer’s argument is whether an AKS violation requires corrupt intent. Background.

Manufacturing 83

Manufacturing Patient-Centered Healthcare Utilities 83

FDA Law Blog

JANUARY 6, 2022

Clinical treatment facility” is defined as “a medical setting, other than a hospital, that provides detoxification, risk reduction, outpatient treatment and care, residential treatment, or rehabilitation for substance use, pursuant to licensure or certification under State law.” 18 U.S.C. § 18 U.S.C. § 18 U.S.C. § 24(b) (emphasis added).

Lab Testing 52

Lab Testing Referral Individual Patient-Centered 52

FDA Law Blog

JUNE 12, 2023

PFI expressed some of its frustration with the current state of regulation of pet food by individual states in its comments on the Center for Veterinary Medicine (CVM) Virtual Public Meeting FDA and the AAFCO Animal Feed Ingredient Definition Process. Enforcement for these regulations also occurs both by federal and state officials.”

Manufacturing 45

Manufacturing Individual Government Illness 45

FDA Law Blog

AUGUST 8, 2024

Governors, state cannabis regulators, law enforcement groups and local governments weighed in, as did marijuana advocates and opponents, marijuana industry associations, Members of Congress, federal law enforcement groups, healthcare and human rights groups, unions and trade associations, and private individuals. 21 U.S.C. §

Government 59

Government Medical IT Manufacturing 59

FDA Law Blog

JANUARY 31, 2022

In addition, the Complaint alleges inappropriate dispensing to numerous individuals, multiple DEA recordkeeping violations, improper alteration of prescriptions, and violations Texas law and federal corresponding responsibility obligations required of pharmacists that dispense opioid prescriptions.

Government 40

Government IT Provider Healthcare 40

FDA Law Blog

MARCH 9, 2023

Our firm has a great deal of experience in pleading with the Government not to prosecute clients that have discovered serious misconduct by employees (including management) and disclosed it to the Government voluntarily. Many federal agencies do have policies that provide a safe harbor for voluntary disclosures, but FDA does not.

Government 52

Government Provider IT Individual 52

FDA Law Blog

JANUARY 31, 2023

Second, FDA did not and still does not have any patent law expertise in-house but our sister agency, NIH, did and does, and so I worked with NIH patent counsel to come up with a sample affidavit that a corporation’s patent counsel could provide to FDA that would affirm that the drug in question could not qualify for a US patent. IT is REAL!

Patients 59

Patients Patient-Centered Government IT 59

FDA Law Blog

NOVEMBER 6, 2023

The LMG Life Sciences awards are based on case evidence and feedback from clients and peers and selected by the editors to provide attorneys and law firms with information on the legal market and the U.S. They range from individuals and start-up companies with no in-house legal staff to large multinational corporations. Karst , Alan M.

Government 40

Government Provider Medical Individual 40

FDA Law Blog

NOVEMBER 2, 2023

These standards would be developed outside the Federal government, leveraging the expertise of the private sector. It finalized a draft guidance published in 2022. Although fairly short and light on substance, it has the potential to reshape the industry in ways that are sorely needed.

Provider 59

Provider Screening IT Government 59

FDA Law Blog

AUGUST 4, 2022

The approval process, pre-approval concerns, product labeling, clinical trials, adverse events reports, patent concerns, and exclusivity – these are all critical aspects in the commercialization process for drugs and biologics that are governed by the FDA.

Government 40

Government Clinic Individual Provider 40

FDA Law Blog

JANUARY 6, 2022

Clinical treatment facility” is defined as “a medical setting, other than a hospital, that provides detoxification, risk reduction, outpatient treatment and care, residential treatment, or rehabilitation for substance use, pursuant to licensure or certification under State law.” 18 U.S.C. § 18 U.S.C. § 18 U.S.C. § 24(b) (emphasis added).

Lab Testing 40

Lab Testing Individual Referral Patient-Centered 40

FDA Law Blog

FEBRUARY 13, 2025

FDA provides definitions for the three datasets. The update procedures should include plans for required labeling changes and training provided to end users. Consistent with the draft guidance, it contains a significant level of detail on the fundamental principles that should govern the design and development of AI-based software.

Manufacturing 71

Manufacturing Management Specialization Provider 71

FDA Law Blog

OCTOBER 10, 2022

The final guidance therefore may have significant implications for a wide range of stakeholders, including not only software developers but also health care providers, hospitals, patients and payors. The guidance provides no rationale for hinging the device status of CDS software on the frequency with which medical information is collected.

Clinic 52

Clinic Medical Provider Patients 52

FDA Law Blog

SEPTEMBER 6, 2022

As the new Federal Register notice explains, FDA issued the 2016 Guidance in question and answer format to respond to the most frequently asked questions about charging for investigational drugs provided under an IND for either clinical trials or expanded access for treatment use under 21 CFR section 312.8. Changes from the 2016 Guidance.

Clinic 52

Clinic Manufacturing Patients IT 52

FDA Law Blog

JUNE 16, 2023

The statement must itemize the cost components related to production of the drug, identify increases in materials or manufacturing costs, and provide other information that the manufacturer believes relevant to determining whether a violation has occurred. SF 2744 also provides a private right of action to enforce the prohibition.

Manufacturing 45

Manufacturing Provider Consulting IT 45

FDA Law Blog

JUNE 27, 2024

The government’s expert testified that any red flag associated with a controlled substance prescription must be resolved and that resolution documented before dispensing. By Larry K. Coconut Grove Pharmacy; Decision and Order, 89 Fed. 50,372 , 50,377 (June 13, 2024). make a record of its resolution, assuming it is resolvable.”

Insurance 52

Insurance Patients Utilities Chronic Condition 52