The US Food and Drug Administration (FDA) has made several changes to its guidances for transitioning medical devices and diagnostics from COVID-related authorization to traditionally marketed ...

A bipartisan pair of U.S. senators have filed a bill to reduce regulations on farmers that grow industrial hemp for ...

Adderall, Ozempic, albuterol, antibiotics and lifesaving cancer meds are in short supply. Here are answers to some of the ...

A former FDA official told lawmakers that dysfunction within the agency exacerbated last year's nationwide infant formula ...

Analysis-In US Abortion Pill Case, FDA Could Soften Blow of Court-Ordered Restrictions By Julia Harte, Gabriella Borter and Brendan Pierson (Reuters) - A conservative federal judge in Texas could ...

with its attendant public health restrictions. According to reports by Reuters yesterday, the United States had said vaccines that are Food and Drug Administration (FDA)-authorised/approved or ...

FMCSA’s Drug and Alcohol Clearinghouse can be confusing for some drivers. Here’s what you need to know to register and ...

With the rapid rise of the specialty drug market, manufacturers are increasingly relying on new advances used by patient hubs ...

Tolterodine market outlook (2023-2030) provides a thorough analysis of the market's current state, including factors such as ...

Under FDA statutes and regulations, drug approval withdrawal generally begins with an informal hearing, which can entail extensive document preparation and the convening of an advisory committee.