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From GRP to SIUU – the Evolution of FDA Guidance on Off-Label Dissemination of Scientific Information

FDA Law Blog

Previous iterations of this guidance from 2009 and 2014 (blogged on here and here ) were known as Good Reprint Practices (GRP). Creation of a “Safe Harbor” for Firm-Generated Presentations of Scientific Information FDA acknowledges that firms may develop presentations of scientific information from an accompanying reprint.

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Screening for Dementia: A Podcast with Anna Chodos, Joseph Gaugler and Soo Borson

GeriPal

Joe 18:38 Yeah, you know, it’s interesting, Soo, I’m doing a county by county visit here in Minnesota where I actually give a presentation on the basics of dementia and Alzheimer’s disease. I don’t have access to change the levers of government. Eric 19:56 Okay, but I’m a primary care provider.

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Endocrinology, Diabetes and Metabolism Board Meeting Summary | Spring 2025

ABIM

See the discussion on the Special Consideration IMG (International Medical Graduates) Pilot Pathway below.) Dr. McDonald spoke about ABIM’s work engaging early career physicians (those who earned initial certification within the last 10 years), including presentations and listening sessions at recent national meetings.

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Infectious Disease Board Meeting Summary | Spring 2025

ABIM

They discussed an interest in its ability to collect data specific to practice areas like HIV and geographic areas—like practice ZIP codes—to better understand workforce needs and patterns. Community Practice in ABIM Governance* Erica N.

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Nephrology Board Meeting Summary | Spring 2025

ABIM

Lieske, MD , raised concerns about how new government policies may affect international medical graduates and health equity work at ABIM. Reddy, MPH, Senior Research Associate for ABIM, reviewed aggregate data gathered so far related to nephrologists, including practice setting, practice size and physician ownership of practices.