Sept 8 (Reuters) - (This Sept. 8 story has been corrected to add the missing words 'from the risks' to the FDA statement, in paragraph 7) The U.S. Food and Drug Administration plans to fast-track ...

The FDA will put three psychedelic drug programs on an ultra-fast approval track, compressing review timelines from roughly 10 to 12 months to as little as one to two months. The agency announced in ...

The Food and Drug Administration announced on Thursday the first round of experimental drugs to be included in a priority voucher program. This FDA initiative is designed to expedite drug review ...

The Honolulu Department of Planning and Permitting has launched a new program to fast-track eligible building permit applications using an artificial intelligence-assisted screening platform ahead of ...

Oct 3 (Reuters) - The U.S. Food and Drug Administration said on Friday it has launched a new pilot program to speed up the review process for generic drugs that are tested and manufactured entirely in ...

On October 8, Maryland Securities Commissioner Melanie Senter Lubin announced a Fast-Track Program, launching January 1, to expedite franchise renewal registrations. The program will benefit ...

FILE PHOTO: Signage is seen outside of the Food and Drug Administration (FDA) headquarters in White Oak, Maryland, U.S., August 29, 2020. REUTERS/Andrew Kelly//File Photo Dec 9 (Reuters) - The U.S.

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.

(Reuters) -The U.S. Food and Drug Administration plans to fast-track reviews of four tobacco firms' nicotine pouches in a pilot program launching on Monday, amid pressure from the Trump administration ...