Plum Health

AUGUST 20, 2023

These medical students will be immersed in the Detroit community over the next 4 years, and upon graduation, many of them will continue to serve the Detroit and Metro Detroit community. WSU SOM’s incoming class of 2026 had 300 Students, with 192 in-state and 108 out-of-state students.

Medical Student 52

Medical Student Community Specialization Medical 52

PEMBlog

OCTOBER 31, 2024

However, this large study shows that probiotics do not significantly shorten illness duration, improve symptoms, or reduce the need for additional medical visits. N Engl J Med 2018; 379:2015-2026. Parents often use probiotics, like Lactobacillus rhamnosus GG , hoping to reduce the severity of their child’s gastroenteritis.

Hospital 105

Hospital Illness Patients Provider 105

ABIM

JUNE 20, 2025

ABIM is pleased to announce openings on the Board of Directors , ABIM Council and several Specialty Boards for initial three-year terms beginning July 1, 2026. Applications are due Sunday, July 20, 2025. ABIM Governance provides a meaningful and rewarding opportunity to join outstanding colleagues in service to the profession and to patients.

Government 40

Government Board-Certified Internal Medicine Community 40

FDA Law Blog

FEBRUARY 21, 2024

By Véronique Li, Senior Medical Device Regulation Expert & Ana Loloei & Allyson B. It is intended to reduce regulatory burdens on medical device manufacturers and importers by enhancing global harmonization in device regulation. The final rule emphasizes risk management activities and risk-based decision making.

Manufacturing 59

Manufacturing Management Medical IT 59

FDA Law Blog

SEPTEMBER 22, 2024

Complaints FDA discussed how LDT developers should handle the transition from the current Quality System Regulation (QSR)(21 CFR Part 820) to the recently promulgated Quality Management System Regulation (QMSR) that is scheduled to take effect on February 2, 2026. By Steven J. Gonzalez & Lisa M.

Manufacturing 64

Manufacturing Electronics Provider Management 64

FDA Law Blog

FEBRUARY 2, 2025

The rules include changes to the notification process, medication packaging, the handling of reports, and safety issues. California pharmacists are still able to provide the oral therapeutics without requiring you to visit your primary care physician through January 1, 2026. See rule at 20 CSR 2220-2.013.

Primary Care Physician 59

Primary Care Physician Primary Care Diagnosis Provider 59

FDA Law Blog

APRIL 14, 2022

Cato — On March 22, FDA announced that it reached agreement with representatives from the medical device industry on proposed recommendations to Congress for the fifth reauthorization of the Medical Device User Fee Amendments (MDUFA V). By McKenzie E. MDUFA V would be applicable to fiscal years 2023 through 2027.

Provider 40

Provider Clinic Medical IT 40

FDA Law Blog

SEPTEMBER 20, 2021

STAR aims to facilitate earlier access to novel uses of existing therapies for patients with a serious condition with unmet medical needs. 31, 2022; CDRP start, FY 2023; Public workshop, by July 31, 2025; Strategy document published, by April 30, 2026. Notable Dates and Timelines – Applications open, Q4 of FY 2023.

Patient-Centered 52

Patient-Centered Manufacturing Clinic Provider 52

FDA Law Blog

FEBRUARY 13, 2025

Baumhardt, Principal Medical Device Regulatory Expert FDA recently released its final guidance for Predetermined Change Control Plans (PCCPs) for Artificial Intelligence-Enabled Device Software Functions (AI-DSF). In such cases, performance testing may be conducted again.

Manufacturing 71

Manufacturing Management Specialization Provider 71

ABIM

JUNE 4, 2025

See the discussion on the Special Consideration IMG (International Medical Graduates) Pilot Pathway below.) Representatives from the American Association of Clinical Endocrinology (AACE), the Association of Program Directors in Endocrinology, Diabetes and Metabolism (APDEM) and the Endocrine Society joined for a portion of the meeting*.

Diabetes 52

Diabetes Board-Certified Telehealth Government 52

ABIM

JUNE 11, 2025

This is now being reviewed by the American Board of Medical Specialties, which oversees ABIM. Johnson, MD, FACP, FIDSA , Senior Vice President for Academic and Medical Affairs, led a discussion with the Infectious Disease Board on community practice in the specialty to create a more inclusive understanding of its role and scope.

Board-Certified 52

Board-Certified Government Community Education 52

ABIM

JUNE 24, 2025

The group discussed policy shifts and potential implications for graduate medical education and health equity. Dr. McDonald acknowledged that recent executive orders have emphasized more competition in medical and legal education accreditation, but reaffirmed ABIM’s commitment to evidence-based practice and health equity.

Board-Certified 40

Board-Certified Board-Certified Physicians Government Community 40

Alabama Academy of Family Physicians

FEBRUARY 19, 2025

Running from February 4 to May 15, this session promises to bring substantial changes to medical consent laws, Medicaid coverage, rural hospital funding, taxation on essential goods, and the transparency of healthcare costs. SB 58 & 101 – Age of Medical Consent Bill What’s in the Bill: Sponsored by Sen.

Insurance 130

Insurance Hospital Management Vaccination 130

ABIM

MAY 30, 2025

Lieske, MD , raised concerns about how new government policies may affect international medical graduates and health equity work at ABIM. One notable trend was a higher representation of international medical graduates and osteopathic physicians in the specialty. Rodriguez, MD , Chair of the Nephrology Board, and John C.

Board-Certified 40

Board-Certified Government Internal Medicine Private Practice 40

FDA Law Blog

JULY 7, 2024

The guidance restates the central premise of the final rule, i.e., that LDTs are medical devices and the clinical laboratories that design, manufacture and use them to test patient specimens are manufacturers. 803), Reporting of Corrections and Removals (21 C.F.R. § 806) and Complaint Files (21 C.F.R.

Manufacturing 64

Manufacturing Provider Physicals Electronics 64

GeriPal

APRIL 3, 2025

I will always, as always, say, you know, you’re welcome to do this in 2026. We covered: The first parody song I wrote, for AGS 2018 in Orlando , about this article by Nancy Schoenborn on how to discuss stopping cancer screening. So this is something. This is the plenary to attend. It is a sold out crowd. Of course. We will step aside.

IT 64

IT Hospital Screening Patients 64

FDA Law Blog

JUNE 14, 2023

By Philip Won & Véronique Li, Senior Medical Device Regulation Expert — “Total Product Life Cycle Advisory Program or TAP pilot — the most exciting thing in MDUFA V. Given Dr. Shuren’s propensity to use the phrase, we have yet to see it formally defined by CDRH.

Manufacturing 45

Manufacturing Medical Appointment Patient-Centered 45

FDA Law Blog

NOVEMBER 21, 2022

The TAP Pilot is intended to “de-risk the medical device valley of death,” the metaphorical place where innovative technologies die while trying to reach the market. Devices in the Safer Technologies Program (STeP) will be included in FY 2026. By Adrienne R. here ), Federal Register notice ( here ) and the Program Website ( here )).

Medical 59

Medical Patient-Centered Provider IT 59

FDA Law Blog

NOVEMBER 17, 2022

The TAP Pilot is intended to “de-risk the medical device valley of death,” the metaphorical place where innovative technologies die while trying to reach the market. Devices in the Safer Technologies Program (STeP) will be included in FY 2026. here ), Federal Register notice ( here ) and the Program Website ( here )).

Patient-Centered 69

Patient-Centered Provider Medical IT 69

FDA Law Blog

FEBRUARY 4, 2025

With the current lapse in authorization, FDA may only award RPD PRVs for applications that have received an RPD designation before December 20, 2024, andunless reauthorized before thenmay not award any RPD PRVs after September 30, 2026. Below, we discuss some of its downstream impacts on the PRV landscape.

IT 52

IT Vaccination Manufacturing Medical 52

FDA Law Blog

AUGUST 14, 2022

The number will begin in 2026 with 10 drug covered under Medicare Part D and will increase annually to 20 Part B and 20 Part D drugs by 2029 and thereafter, with the selected drugs accumulating from year to year.

Manufacturing 98

Manufacturing Government Vaccination Utilities 98

Physician's Weekly

JUNE 26, 2025

In the medical odyssey that followed, she suffered double vision, chronic nausea, brain fog, and profound weakness. The HHS budget proposal for fiscal year 2026 makes no mention of vaccine safety programs. Once a rock climber, she became a couch potato. Kennedy Jr. forced him out in May. The current U.S.

Vaccination 52

Vaccination Patient-Centered Government IT 52

FDA Law Blog

FEBRUARY 20, 2025

In contrast, AMP and ACLA both asserted that the rule would harm medical care. The first phase of the rule, which takes effect in less than three months, requires laboratories to have certain policies and procedures in place to begin handling complaints, reporting Medical Device Reports, and reporting corrections/removals. It did not.

Patient-Centered 102

Patient-Centered Consulting Government Clinic 102

Physician's Weekly

JUNE 25, 2025

Dangerous changes loomed: To compensate for tax cuts for the wealthy, Trump’s “big, beautiful” bill and budget proposal for fiscal year 2026 threaten to curtail Medicaid, which provides health coverage for people with low incomes and disabilities. In a few days, he would drive from Mississippi to Washington, D.C.,

Government 52

Government Community Families Family 52