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AAFP Represents Members During 2025 Legislative Session

Alabama Academy of Family Physicians

By engaging with lawmakers and key stakeholders, the Academy worked to ensure that the voices of family physicians were heard in discussions that have the potential to impact healthcare delivery and access for communities across the state. What Happened: This legislation has been enacted into law.

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The Most Engaging Decision You’ll Read All Year – Five Stars

FDA Law Blog

FDA , Petitioners, a liquid nicotine manufacturer, sued FDA arguing that the Agency was arbitrary and capricious in rejecting the Petitioner’s Premarket Tobacco Application (“PMTA”) in violation of the Administrative Procedure Act (“APA”). FDA also directed manufacturers to produce detailed marketing plans.

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How Gut Health and Digestion Influence Cholesterol Levels

Imperial Center Family Medicine

The liver manufactures new cholesterol molecules and captures excess from circulation for excretion. By regularly incorporating prebiotic foods or supplements into your diet, you effectively help feed and cultivate communities of ideal commensal flora adept at beneficial cholesterol conversions.

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Baby Formula Shortages

Georgetown Pediatrics & Family Medicine

If not, your pediatrician’s office can work with you to access all community resources. Always mix formula as directed by the manufacturer. If you have any concerns about your baby’s nutrition, please talk with your pediatrician. What if baby formula is out of stock everywhere I look? Check social media groups.

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PhRMA Sues Arkansas for Meddling in the Federal 340B Drug Discount Program

FDA Law Blog

By Faraz Siddiqui — Last week, we blogged about a growing list of drug manufacturers that have refused to follow a 2010 guidance issued by the Health Resources and Services Administration (“HRSA”), which permits 340B covered entities to contract with multiple pharmacies to dispense drugs to covered entity patients. 23-92-604(c)(1), (2).

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FDA Draft Guidance: Everything You May Want to Know about OMUFA Fees

FDA Law Blog

The facility fee applies to a single manufacturing facility. The guidance explains that a facility counts as a single facility subject to a single facility fee if it is under one management and in one geographic location and address, and is engaged in manufacturing or processing the finished dosage form of an OTC monograph drug product.

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Urinary Incontinence Revisited: George Kuchel & Alison Huang

GeriPal

On our last podcast about urinary incontinence the song request was, “Let it go.” This time around several suggestions were raised. Eric suggested, “Even Flow,” by Pearl Jam. Someone else suggested, “Under Pressure,” but we’ve done it already. We settled on, “Oops…I did it again,” by Britney Spears. I suggested even flow. That’s a good one.

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