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Green Practice News: April 2025

My Green Doctor

According to the 2023 report of the Lancet Countdown, mortality caused by extreme heat events increased by 53.7% Behavior Change Happens in the Exam Room Unlike government agencies or corporations, healthcare professionals speak directly to individuals in a trusted, one-on-one setting. Need help planning an event?

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FIFA Cases Hold Lessons for FDA-Regulated Companies – Organizations can be Victims of Their Own Employees’ Criminal Conduct

FDA Law

To hold a corporation liable for these actions, the government must establish that the corporate agent’s actions (i) were within the scope of his duties and (ii) were intended, at least in part, to benefit the corporation. In light of the above, the government generally resists the notion that an organization is a victim of its own employees.

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15 Years Strong: Rare Disease Week’s Remarkable Journey of Support

FDA Law

What started as a day has — due to its popularity and the persistent efforts of patients and industry — evolved into a week-long event. And my support and pride continue since we now see a host of programs and events the last week of February playing out around the world.

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Rheumatology Board Meeting Summary | Spring 2025

ABIM

Johnson, MD, FACP, FIDSA , Senior Vice President for Academic Affairs, added that ABIM provides program directors with aggregate performance data in their programs and, with permission, individual graduate data so that program directors can make adjustments to the programs as needed.

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Pet Food Institute Proposes Modernization of Pet Food and Treats Regulation

FDA Law

PFI expressed some of its frustration with the current state of regulation of pet food by individual states in its comments on the Center for Veterinary Medicine (CVM) Virtual Public Meeting FDA and the AAFCO Animal Feed Ingredient Definition Process. PFI has noted that it is not feasible to develop and label products for an individual state.

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ACI’s FDA Boot Camp – September 14-15, 2022 (Virtual)

FDA Law

The approval process, pre-approval concerns, product labeling, clinical trials, adverse events reports, patent concerns, and exclusivity – these are all critical aspects in the commercialization process for drugs and biologics that are governed by the FDA.

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Podcast: AI, innovation, and value-based care in medicine

Permanente Medicine

I know for a fact that the government or legislators looked to us in Permanente. Also understanding where pharmacies would not be available because of the catastrophes that were going on. So putting that all together to prevent disasters is at the heart of what we’re trying to do. And then putting that on steroids with AI.