Announcing the results of the 2026 INFORMS Board of Directors election and the new board for 2027.
INFORMS has named 12 distinguished leaders as the 2026 class of INFORMS Fellows, one of the highest honors in the profession.
Most medical devices do not hit the market through rigorous safety testing but by being deemed similar enough to something already approved—the “predicate” device through a mechanism known as the FDA’s 510(k) pathway. But similar is not a synonym for safe. While the assumption may be that substantial equivalence is a reasonable stand-in for a safety review, a share of devices cleared with this method still get recalled, and the FDA spends valuable time reviewing devices the same way, regardless of how risky it is on paper.
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At least 1,303,390 people in North Carolina have tested positive for the coronavirus, and at least 15,247 have died since March 2020, according to state health officials.
The U.S. Food and Drug Administration (FDA) developed its Accelerated Approval Program in 1992, with the intention of moving certain new drugs to the market faster.
During the heights of the pandemic, COVID-19 outbreaks were frequently reported among fire departments, with one Johnston County department hit by the death of a firefighter as well as several hospitalizations.
Consumers could soon get discounted coronavirus tests at Amazon, Kroger and Walmart as part of President Joe Biden's plan to significantly increase testing.
Sept 12 (Reuters) - Yet another billionaire entrepreneur is set to ride into space this week, strapped inside the capsule of a SpaceX rocketship as part of an astro-tourist team poised to make history as the first all-civilian crew launched into Earth orbit.
OR/MS Today is the INFORMS member magazine that shares the latest research and best practices in operations research, analytics and the management sciences.
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Analytics magazine showcases articles and research reports based on big data, AI, machine learning, data analytics and other new-age technologies.
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