ABIM

JUNE 30, 2025

The Specialty Board discussed the LKA in greater detail, as well as the use of artificial intelligence (AI) in assessment development and the integration of public members in ABIM Governance. Preliminary data gathered to date indicate that 92% of gastroenterologists are clinically active, with nearly half (46.7%) in private practice, 25.1%

Board-Certified 52

Board-Certified Government Community Internal Medicine 52

ABIM

JUNE 12, 2025

McDonald shared more about a pilot model announced last year that would create a pathway for exceptionally qualified international medical graduates (IMGs) successfully completing ACGME-accredited subspecialty fellowship to become Board eligible in Internal Medicine and subspecialties. Community Practice in ABIM Governance* Erica N.

Board-Certified 52

Board-Certified Internal Medicine Government Community 52

Permanente Medicine

MAY 22, 2025

As chief quality officer at The Permanente Federation, Dr. Bridges oversees coordination of national clinical quality care programs across Kaiser Permanente for its 12.6 The Federation is the national leadership and consulting organization for Permanente Medical Groups and their more than 25,000 physicians. million members.

Appointment 52

Appointment Board-Certified Patient-Centered Integrated Care 52

Annals of Family Medicine

NOVEMBER 20, 2024

Context: Health Technology Assessment (HTA) organizations determine the value of health technologies such as medical devices, lab tests, or medications. learning), the use of guideline-based information in clinical practice, and subsequent patient health outcomes. Health organization outcomes.

General Practitioner 130

General Practitioner Lab Testing Relationship Family Physician 130

My Green Doctor

MAY 3, 2025

In This Issue : Why Renewable Energy Belongs in Every Clinic Medical Waste: One Model for Improvement OnTrack with your Sustainability Goals? Powering Health, Protecting the Planet – Why Renewable Energy Belongs in Every Clinic Healthcare professionals have always been trusted voices on public health.

Healthcare 52

Healthcare Healthcare Professional Consulting Management 52

FDA Law

JANUARY 18, 2022

Cato — On December 10, 2021, FDA issued a discussion paper titled 3D Printing Medical Devices at the Point of Care seeking feedback on FDA regulatory oversight of various 3D-printing scenarios, in order to inform future policy development. products intended for medical purposes). products intended for medical purposes).

Medical 98

Medical Manufacturing Healthcare Government 98

My Green Doctor

APRIL 4, 2025

New Research: Teaching Patients about Climate Resilience Newly published original research co-authored by My Green Doctor’s Dr. Todd Sack concludes that, “ the medical office waiting room appears to be an accepted, time-efficient, and effective site to communicate knowledge on climate change and health. ” of total U.S.

Healthcare Professional 52

Healthcare Professional Healthcare Community Medical Advice 52

The Direct Doctors Difference

AUGUST 18, 2021

According to DPC Frontier, a site owned by a DPC physician/lawyer who was a founder of the movement, there are now over 1500 clinics doing pure Direct Care across the nation. Clinics are often owned by solo doctors or, as in the case of Direct Doctors, by 2-3 physicians in a small group practice.

Primary Care 52

Primary Care Healthcare Insurance Government 52

Common Sense Family Doctor

MARCH 18, 2025

Smith, a general internist and professor of medicine and psychiatry at Michigan State University, explains why our medical system consistently prioritizes physical over emotional health and presents some ambitious proposals for how to rectify this harmful disparity. This relatively slim volume is divided into three parts.

Mental Health 52

Mental Health IT Primary Care Primary Care Physician 52

PEMBlog

JUNE 7, 2023

There are protocols in place that assist highly trained Emergency Medical Service providers in assuring that agitated children are safely transported to their destination. Government. NASEMSO: Clinical care and restraint of agitated or combative patients by emergency medical service practitioners. Prehosp Emerg Care.

Transportation 122

Transportation Patient-Centered Management Finance 122

FDA Law

JANUARY 18, 2022

Cato — On December 10, 2021, FDA issued a discussion paper titled 3D Printing Medical Devices at the Point of Care seeking feedback on FDA regulatory oversight of various 3D-printing scenarios, in order to inform future policy development. products intended for medical purposes). products intended for medical purposes).

Medical 75

Medical Manufacturing Healthcare Government 75

ABIM

APRIL 24, 2025

Chrostowski, DNP, APR-N, ANP-C , asked whether ABIM will offer continuing medical education (CME) credits through the LKA. Thousands of activities are eligible for both MOC and CME via a collaboration with the Accreditation Council for Continuing Medical Education at cmepassport.org.

Board-Certified 40

Board-Certified Board-Certified Physicians Community Government 40

FDA Law

NOVEMBER 6, 2023

Admittedly, BiMo inspections (into items like adequacy of bioequivalence data, consistency of clinical trial data with medical records, and compliance with clinical trial protocols) lend themselves better to an RIE than assessing manufacturing compliance with regulatory requirements. We should explain what RIEs are.

Manufacturing 105

Manufacturing Clinic IT Utilities 105

FDA Law

OCTOBER 10, 2022

Javitt — On September 28, 2022, the FDA issued the long anticipated final Clinical Decision Support Software Guidance (CDS Guidance), which replaces the revised draft guidance document from 2019. Criterion 2 : Non-Device CDS software functions display, analyze or print medical information about a patient or other medical information.

Clinic 52

Clinic Medical Provider Patients 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. Digital uptake is more prevalent in high-volume and urban hospital networks.

Patient-Centered 40

Patient-Centered Provider Clinic Patients 40

FDA Law

AUGUST 4, 2022

In September 2020, the Agency issued an unfavorable advisory opinion to Pfizer, concluding that the proposal was “highly suspect” under the AKS “because one purpose of the [proposed program]—perhaps the primary purpose—would be to induce Medicare beneficiaries to purchase [Pfizer’s] federally reimbursable Medications.”

Manufacturing 98

Manufacturing Medical Government IT 98

FDA Law

JULY 24, 2023

This time, rather than use codes and patent certifications, the fight is over orphan drug exclusivity (“ODE”), with Jazz challenging FDA’s clinical superiority decision concerning sodium oxybate in the treatment of narcolepsy. 360cc(c), the statute does not permit FDA to promulgate regulations to use clinical superiority to break ODE.

Clinic 52

Clinic Provider IT Patients 52

FDA Law

MARCH 3, 2024

This proposed legislation should be of interest to any biotechnology companies that want to do business with the federal government in the future. Scope Part 2 —Is reimbursement under Medicaid a grant of funds by the federal government, such that they are governed by the Act? House of Representatives ( H.B.

Manufacturing 102

Manufacturing Government Consulting IT 102

Physician's Weekly

JUNE 24, 2025

Robin Wolaner, 71, a retired publisher in Sausalito, California, has been known to badger friends who delay getting recommended shots, sending them relevant medical studies. has long disparaged certain vaccines, calling them unsafe and saying that the government officials who regulate them are compromised and corrupt. Kennedy Jr.,

Vaccination 52

Vaccination Illness Hospital Patient-Centered 52

FDA Law

JUNE 2, 2025

Mullen At midnight on Friday, May 30, 2025, the governments deadline to notice an appeal from the U.S. District Court for the Eastern District of Texass decision vacating the LDT Rule lapsed without the government doing so. RUO-labeled reagents and materials are often used in LDTs in clinical laboratories. By Steven J.

IT 64

IT Manufacturing Government Clinic 64

PEMBlog

JUNE 14, 2023

This episode is a co-production of the Emergency Medical Services for Children Innovation and Improvement Center whose mission is to minimize morbidity and mortality of acutely ill and injured children across the emergency continuum. Government. PMID: 32393605. American Journal of Emergency Medicine. Doi.org/10.1016/j.ajem.2020.11.021

Mental Health 98

Mental Health Management Patient-Centered Illness 98

Permanente Medicine

MAY 20, 2025

Khang Nguyen, MD, chief transformation officer of the Southern California Permanente Medical Group, discusses how AI can increase clinicians’ joy in medicine and improve patient outcomes with Chris Grant, chief operating offer and executive vice president of Kaiser Permanente, The Permanente Federation, and host of the Permanente Medicine Podcast.

Patient-Centered 52

Patient-Centered Patients IT Medical 52

The Clinical Problem Solvers

NOVEMBER 22, 2021

10:37 “Blood quantum” and the burden of proof 18:05 Challenges of Indigenous Peoples in medical spaces 24:50 COVID-19 and climate change’s impact on Indigenous Peoples 30:27 Racism in academia and creating safe spaces 41:22 “Data genocide” 50:11 What can listeners do going forward?

Community 52

Community Patient-Centered Medical Student Medical 52

Tiny Physician

FEBRUARY 15, 2022

However, the core problem in our medical system is yet to be addressed which actually results in these unfortunate incidents. Only very few hospitals and medical colleges have Public Relations Officers (PROs) at all the ICUs and major wards to talk with the patients and to sort out these problems.

Patient-Centered 52

Patient-Centered Government Referral Hospital 52

FDA Law

FEBRUARY 4, 2024

Mullen — On January 18, 2024, the director of FDA’s Center for Devices and Radiological Health and the chief medical officer and acting director of CMS’ Center for Clinical Standards and Quality issued a joint press release supporting FDA’s recent proposed rule regulating Laboratory Developed Tests (LDTs). Gonzalez & Gail H.

Clinic 59

Clinic Management Medical IT 59

FDA Law

OCTOBER 24, 2023

By Dara Katcher Levy — Yesterday, FDA published a new Draft Guidance, “ Communications from Firms to Health Care Providers Regarding Scientific Information on Unapproved Uses of Approved/Cleared Medical Products Questions and Answers ” (SIUU Guidance or Draft Guidance).

Clinic 64

Clinic Clinical Practice Provider Utilities 64

FDA Law

JANUARY 12, 2025

FDAs interpretation of several threshold criteria for eligibility (serious condition, available therapy, unmet medical need) will continue to rely upon the 2014 Guidance. an intermediate clinical endpoint) and that is reasonably likely to predict an effect on irreversible morbidity or mortality or other clinical benefit.

Clinic 64

Clinic Relationship Provider IT 64

FDA Law

JANUARY 5, 2023

In mid-November, FDA collaborated with the MITRE Corporation to publish an update to the Medical Device Cybersecurity Regional Incident Preparedness and Response Playbook. Combination products are sharing the digital moment with those classified solely as medical devices.

Manufacturing 59

Manufacturing Patient-Centered Provider Telehealth 59

Georgetown Pediatrics & Family Medicine

MAY 11, 2022

They may have samples in stock, connections to other local organizations, or ideas of other places to call, such as your local WIC clinic. I heard the government will be importing baby formula from other countries. Call your pediatrician if you cannot access the formula you need for your baby. Is that safe?

Supply Chain 52

Supply Chain Specialization IT Family Medicine 52

Blood, Sweat, and Tears

MAY 24, 2022

You have to be able to laugh at situations, the system, the government, people and especially yourself (Mostly yourself). She would peer out at the gate of the clinic and start predicting what cases we would see. So you came to the clinic after you went out to get yourself damaged? I’m not sure why. Everyone was happy.

Referral 52

Referral Community Patients Specialization 52

Tiny Physician

JULY 3, 2022

Homeopathy is a pseudoscientific medical stream that originated in Germany. Randomized controlled trials which were published in renowned medical journals have proven beyond doubt that homeopathy has no effects. However, homeopaths have the tendency to make medicines from any substance and no government authority questions them.

Relationship 52

Relationship Government IT Physicals 52

FDA Law

AUGUST 29, 2021

The federal government does its own version of rebranding with each change in administration. clinical testing of implanted brain computer interface devices for patients with paralysis or amputation), enforcement (e.g., Walsh & JP Ellison — Companies often use rebranding to reposition and refocus their business.

Government 52

Government Electronics IT Clinic 52

33 Charts

OCTOBER 2, 2021

And as suggested recently in the New England Journal of Medicine , One of the most important factors at play in the clinical environment is the apparent tension between availability and attention. The zero-sum medical day In many healthcare systems the Epic feature is turned on and health professionals are expected to respond.

Patients 75

Patients IT Provider Family Doctor 75

GeriPal

JULY 19, 2024

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. What hasn’t been shown, Eric, is that if you apply tools like this, clinical outcomes down the road are better for patients.

Screening 119

Screening Primary Care Patient-Centered IT 119

FDA Law

OCTOBER 25, 2021

The Medical Device Amendments of 1976 created the initial premarket application (PMA) review and 510(k) substantial equivalence review processes. Only a year later, in 1977, FDA promulgated regulations governing 510(k) reviews (21 C.F.R. befitted a very important pathway to market for novel medical devices.

Manufacturing 52

Manufacturing Specialization Government IT 52

FDA Law

JANUARY 6, 2022

In general, EKRA prohibits, knowingly and willfully, soliciting, receiving, paying or offering kickbacks in exchange for referring to, inducing a referral to, or using the services of a recovery home, clinical treatment facility, or laboratory. 18 U.S.C. § 18 U.S.C. § 18 U.S.C. § 18 U.S.C. § 24(b) (emphasis added). 18 U.S.C. § 220(b)(2).

Lab Testing 52

Lab Testing Referral Individual Patient-Centered 52

FDA Law

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