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 ...

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.

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 ...

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 ...

Healthcare generates massive volumes of data daily – from electronic health records and insurance claims to genomic research and wearable devices. Recent analyses from RBC Capital Markets estimate ...

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Teradata is introducing the Teradata Factory, extending the Teradata Autonomous Knowledge Platform with a fully integrated on-premises foundation for enterprises running AI and analytics in hybrid ...

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Arctera announced its transition to a focused SaaS operating model, removing traditional constraints on data volume, users, and environments, and enabling enterprises to apply consistent compliance ...