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Maryland's Primary Care Program: incremental progress or breakthrough?

The Health Policy Exchange

Our residency, formerly a collaboration with Providence Hospital, is now known as the Medstar Health/Georgetown-Washington Hospital Center Family Medicine Residency Program. According to MedChi , the average practice received $176,000 in care management fees in 2019. I stepped down as director of the Robert L. Phillips, Jr.

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How Mental Health & SUD Bias Impact ED Physical Care

Physician's Weekly

“This study uncovered negative and positive provider, treatment, and system-related factors that contribute to these patients’ experiences and offered recommendations for improving care experiences.” Provide printed “What to Expect” one‑pagers at registration to align patient expectations with ED capabilities. Clarify ED scope.

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Using technology to reclaim our time

Today's Hospitalist

Since the mid-1990s, our capacity for innovation has never stopped as hospitalists navigate a complex landscape of acute illnesses, interprofessional collaborations and the imperative to provide efficient, high-quality care. We have seen explosive growth and become a cornerstone of modern health care systems.

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Episode 354: Antiracism in Medicine – Episode 25 – Live from SGIM 2024: Best of Antiracism Research at the Society of General Internal Medicine’s 2024 Annual Meeting

The Clinical Problem Solvers

Interconception Care for Primary Care Providers: Consensus Recommendations on Preconception and Postpartum Management of Reproductive-Age Patients With Medical Comorbidities. Clinician Response to Patient Medication Prices Displayed in the Electronic Health Record. During this episode, we hear from Dr. S. Zakaria, S., Vaught, A.

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When Worlds Collide: The Theory of Real-World Evidence Meets Reality

FDA Law

RWD can be collected from a wide range of sources, such as electronic health records, registries, administrative claims, pharmacy data, and feedback from wearables and mobile technology. Rather than looking at how RWD/RWE provide meaningful information on safety and effectiveness, reviewers often focus on perceived gaps.

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DEA Tweaks DEA-222 Supplier Information Requirement

FDA Law

DEA issued a final rule in September 2019 implementing a new single-sheet form to replace triplicate carbon copy DEA Form 222s (“triplicate forms”). Registrants may also use DEA’s electronic Controlled Substance Ordering System (“CSOS”)). 38230 (July 20, 2021). New Single-Sheet Format for U.S. 51368 (Sept. 21 C.F.R § 1305.12(c).

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510(k) Modernization 2023

FDA Law

The electronic Submission Template and Resource (eSTAR) program, which we blogged about here and here , also makes the highlight reel given its aim to improve consistency and efficiency in how 510(k)s are prepared. Baumhardt, Senior Medical Device Regulation Expert & Adrienne R.

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