The Food and Drug Administration, in partnership with STOP Foodborne Illness, a non-profit public health organization, is set ...

U.S. Food and Drug Administration Accepts Bristol Myers Squibb’s Application for Subcutaneous Nivolumab (nivolumab and hyaluronidase) ...

The U.S. Food and Drug Administration on Friday approved the first drug to treat people with potentially deadly food ...

The removal of small amounts of brain tissue from desperately ill patients, done as part of a Mount Sinai research project, ...

The Federal Trade Commission is challenging patents on 20 brand-name drugs, including the blockbuster weight-loss injection ...

Two weeks ago, the Food and Drug Administration approved Xolair (omalizumab) for immunoglobulin E-mediated food allergy in certain adults and children one year or older for the reduction of ...

Food and Drug Administration (FDA) Commissioner Dr. Robert Califf testified on oversight matters before the House Oversight and Accountabili… read more Food and Drug Administration (FDA ...

U.S. Food and Drug Administration (FDA) announced the filing of a food additive petition that asks FDA to remove its approval ...

VMS+4.0 submitted to FDA on May 1 for clearance Ventripoint will market new advances after FDA clearanceTORONTO, Ontario - () - May 6, 2024 - TheNewswire - May 6, 2024 - Ventripoint Diagnostics Ltd. ( ...

First Oral Penem in the U.S. and Second New Oral Treatment for uUTIs in Over 25 Years, if approved-- --Potential Approval Early Q4 2024-- DUBLIN, Ireland and CHICAGO, April 29, 2024 (GLOBE NEWSWIRE) ...

Genomics plc and GSK announced a new collaboration to explore the potential for using polygenic risk scores (PRS) in clinical trials, to improve understanding of disease risk and patient selection ...

Food and Drug Administration (FDA) Commissioner Dr. Robert Califf testified on oversight matters before the House Oversight and Accountabili… read more Food and Drug Administration (FDA ...