CryptoWorld News reports that the FDA (U.S. Food and Drug Administration) plans to accelerate the drug trial process by increasing transparency in clinical trials, utilizing real-time data and artificial intelligence. The agency's Chief AI Officer Jeremy Walsh stated that this proposal could shorten the drug development cycle by "months, or even years." Under this plan, the FDA will monitor macro signals in real-time regarding the effectiveness and safety of experimental drugs, but will not collect all patient-level data. Additionally, the FDA released a notice on Tuesday seeking information on how to use AI to accelerate early clinical research, describing early clinical research as "a critical bottleneck in drug development."

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