The FDA commissioner's effort to shorten the review of drugs favored by the Trump administration is causing alarm across the ...
GlobalData on MSN
FDA and EMA release collaborative AI framework for drug development
"FDA and EMA release collaborative AI framework for drug development" was originally created and published by Pharmaceutical ...
Jan 19 () - Pharmaceutical company Boehringer Ingelheim said on Monday the U. Food and Drug ​Administration had approved its ...
5don MSN
Exclusive: US FDA delays two drug reviews in new voucher program after safety, efficacy concerns
The U.S. Food and Drug Administration has delayed reviews of two drugs chosen for the Trump administration's new fast-track ...
Questions remain among top Food and Drug Administration officials over who has the appropriate legal authority to sign off on ...
At a Food and Drug Administration cell and gene therapy (CGT) roundtable last June, most speakers pushed for the agency to ...
Valneva withdrew its chikungunya vaccine applications following a license suspension and data suggesting a probable link to serious adverse outcomes.
The FDA's orphan drug designation supports LP-284's development for soft tissue sarcomas, addressing significant unmet needs in this adult patient population. The FDA granted orphan drug designation ...
Tri-Union Seafoods initiated the recall after a distributor mistakenly shipped quarantined cans, which were first recalled last February.
The U.S. Food and Drug Administration has delayed reviews of several drugs selected for the Trump administrations new ...
Inquirer.net on MSN
FDA: Lack of food safety limits not a 'shield against accountability'
The Food and Drug Administration (FDA) on Tuesday warned manufacturers that the lack of specific safety limits cannot be used ...
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