Fortress Biotech, Inc. (แนสแด็ก:FBIO) รายงานเมื่อวันจันทร์ว่าผู้ถือหุ้นได้ลงคะแนนเสียงในข้อเสนอห้าข้อในการประชุมประจําปีของบริษัทซึ่งจัดขึ้นเมื่อวันที่ 17 ...

หุ้นสามัญของบริษัทจะยังคงซื้อขายภายใต้สัญลักษณ์เดิมใน ... Cellectar ยังได้รับการกําหนด Fast Track และ Orphan Drug จาก FDA และการกําหนด ...

FDA Commissioner Marty Makary committed to Sen. Josh Hawley that the agency will conduct a safety review of the abortion pill mifepristone.

The FDA and Stealth look set to relitigate the debate, with the biotech planning to file for approval once again. Stealth has laid off 30% of its staff to free up funds for the resubmission.

The FDA has launched the generative AI tool, Elsa, agency-wide to help its employees with everything from clinical reviews to investigations. Sure, we're living in a time of widespread ...

HHS Secretary Robert F. Kennedy Jr. asked the FDA "to review the latest data on mifepristone ," but experts say concerns about the abortion pill's safety are misguided.

Food and Drug Administration (FDA) Commissioner Marty Makary committed to reviewing the abortion drug mifepristone in a letter sent to Sen. Josh Hawley (R-Mo.). “As with all drugs, FDA continues ...

The FDA launched a generative artificial intelligence (AI) tool, dubbed Elsa, designed to help employees such as scientific reviewers and investigators work more efficiently, the agency announced ...

The FDA has updated COVID-19 vaccine regulations. Only people aged 65 and up, along with certain groups, will be eligible to receive booster shots.

The FDA rolled out its agency-wide AI tool weeks ahead of schedule, on Monday offering a look at the technology and how it may be used.

READ: FDA promises to cut by half approval time for new products No hike for decades. The rate of fees and charges of the FDA has not been updated for more than 20 years since the implementation ...

Tomatoes distributed in three southern states are now the subject of a possibly deadly recall, according to the Food and Drug Administration.. The recall, first announced by the FDA on May 2 for ...