California Academy of Family Physicians (CAFP)

MAY 14, 2025

Proposed Changes to Medi-Cal Coverage for Undocumented Individuals Enrollment Freeze for Full-Scope (State-Only) Medi-Cal Expansion to Undocumented Adults – Freezes new enrollment for undocumented adults aged 19 and older, effective January 1, 2026. The policy would be effective January 1, 2026.

Healthcare 204

Healthcare Family Physician Management Individual 204

PEMBlog

OCTOBER 31, 2024

We looked at every outcome we could think of, combined gastroenteritis severity score, duration and severity of diarrhea and vomiting, duration of fever, unplanned healthcare visits, household transmission rates, daycare and work absenteeism. N Engl J Med 2018; 379:2015-2026. N Engl J Med. 2018 Nov 22;379(21):2002-2014. Freedman et al.

Hospital 105

Hospital Illness Patients Provider 105

ABIM

JUNE 11, 2025

Representatives from the Infectious Diseases Society of America (IDSA) and the Society for Healthcare Epidemiology of America (SHEA) joined for a portion of the meeting*. ABIM’s website features expansive sections on research related to assessment and clinical outcomes. The following is a summary of the spring meeting.

Board-Certified 52

Board-Certified Government Community Education 52

ABIM

JUNE 24, 2025

The questionnaire gathers information about clinical work and practice patterns, and ABIM uses the information to help update exam blueprints, develop policies for initial certification and MOC, and ensure adequately diverse representation of the profession in research.

Board-Certified 40

Board-Certified Board-Certified Physicians Government Community 40

FDA Law Blog

JUNE 14, 2023

In FY 2026 – FY 2027, continue to support products enrolled in previous fiscal years and expand to enroll up to 100 additional products each fiscal year within existing OHTs or expand to additional OHTs, depending on lessons learned from FY 2023 – FY 2025 experience (i.e., up to 125 total products enrolled through FY 2025).

Manufacturing 45

Manufacturing Medical Appointment Patient-Centered 45

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. 820.198). .

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. It always has clinical relevance to practice today. And this complete lack of attention to the real needs of persons with dementia is really kind of a shameful part of US healthcare. Of course. We will step aside. Speaker 6 03:29 Andy. Like a song.

IT 64

IT Hospital Screening Patients 64