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Geriatric Medicine Board Meeting Summary | Spring 2025

ABIM

He emphasized ABIM’s focus on patient-centered standards and promoting high-quality care, as well as ABIM’s commitment to ensuring a diverse governance that reflects the physician and patient population. Community Practice in ABIM Governance* Erica N. Above all, they noted the value of evolving definitions and remaining inclusive.

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FDA Abandons Its Defense of the LDT Rule, But is It Signaling an Increase in RUO Scrutiny?

FDA Law

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.

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Many Older People Embrace Vaccines. Research Is Proving Them Right.

Physician's Weekly

has long disparaged certain vaccines, calling them unsafe and saying that the government officials who regulate them are compromised and corrupt. 1, 2013, weren’t eligible for vaccination, but those even slightly younger were eligible. The new studies are coming at a fraught political moment. Kennedy Jr.,

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Rheumatology Board Meeting Summary | Spring 2025

ABIM

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. Learn More Subscribe to the ABIM Blog to stay on top of the latest news.

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The Good, the Bad and the Ugly: New Legislation Would Reform the ANDA Suitability Petition Process and Require Timely Assignment of 505(b)(2) NDA Therapeutic Equivalence Evaluation Codes (“the Good”)

FDA Law

Government Accountability Office report here ). 21, 2013) – establishing the policies and procedures for responding to suitability petitions, and that reiterates that “[u]nder 21 CFR 314.93(e), This bill repeals the requirement to file a suitability petition for ANDAs that do not require clinical data.

IT 40
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The Good, the Bad and the Ugly: New Legislation Would Reform the ANDA Suitability Petition Process and Require Timely Assignment of 505(b)(2) NDA Therapeutic Equivalence Evaluation Codes (“the Good”)

FDA Law

Government Accountability Office report here ). 21, 2013) – establishing the policies and procedures for responding to suitability petitions, and that reiterates that “[u]nder 21 CFR 314.93(e), This bill repeals the requirement to file a suitability petition for ANDAs that do not require clinical data.

IT 40
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Endocrinology, Diabetes and Metabolism Board Meeting Summary | Spring 2025

ABIM

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*. Community Practice in ABIM Governance* Erica N.