Lizzy leads STAT’s coverage of the FDA. Her stories explore the relationship between politics and science at the FDA, industry influence, and the agency’s ability to protect and promote public health.

Why does it take a new drug 10 years, on average, to come to market? Part of the reason lies in the dead time in the process. Historically, trials have required tedious tabulations and repeated ...

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The FDA today announced a new initiative to allow its reviewers to access information from clinical trials in real time, with two major industry players already taking part in a pilot program.

WHITE OAK, MD – The US Food and Drug Administration (FDA) has announced plans for a future pilot program intended to facilitate the real-time review of clinical trials by regulators, as well as the ...

WASHINGTON, April 28 (Reuters) - The U.S. Food and Drug Administration launched a pilot program on Monday aimed at allowing the ‌agency to monitor clinical trial data in real time, a step the agency ...

PocketOS was left scrambling after a rogue AI agent deleted swaths of code underpinning its business It only took nine seconds for an AI coding agent gone rogue to delete a company’s entire production ...

Nasdaq Data Link APIs provide a flexible and efficient method of delivery for real-time exchange data and other financial information. Stock market data is made available through a suite of streaming ...

Investors may trade in the Pre-Market (4:00-9:30 a.m. ET) and the After Hours Market (4:00-8:00 p.m. ET). Participation from Market Makers and ECNs is strictly voluntary and as a result, these ...

Worland is a senior correspondent at TIME, based in the Washington, D.C., bureau and the founder of TIME’s Future Proof newsletter and platform for understanding the climate and energy economy. He ...