News

Federal judge orders Trump administration to unblock pandemic relief money for schools
Officials in sixteen states and the District of Columbia sued in response, leading to Tuesday’s order from U.S. District ...
US FDA advisers to discuss COVID-19 vaccine recommendations on May 22
The U.S. Food and Drug Administration said on Wednesday it will hold a meeting of experts on May 22 to discuss COVID-19 ...
BioSpace4h
Is the New HHS Vaccine Requirement Anti-Vaccine Activism Disguised as Policy?
Yes, according to leading vaccine physician Paul Offit, who denounced the new placebo-controlled trial requirements for ...
Moderna study shows immune response in older adults for a combo flu and COVID-19 shot
A combination shot for flu and COVID-19 using messenger RNA generated antibodies in a study, but U.S. government regulators ...
Critic Of Drug Industry And COVID-19 Measures To Lead FDA Vaccine Program
Dr. Vinay Prasad, a prominent critic of the pharmaceutical industry and the Food and Drug Administration, has been named to ...
Moderna: Combo flu-COVID shot works in older adults
Moderna’s study, involving 8,000 adults 50 and older, showed the new combo shot generated an immune response against COVID and most strains of flu compared to existing stand-alone shots.
Moderna, Pharma Stocks Fall as FDA Names Industry Critic as Top Vaccine Regulator
Biotech and pharmaceutical stocks were sliding Tuesday afternoon as the Food and Drug Administration named Dr. Vinay Prasad, ...
FDA set to meet this month on COVID vaccines
The advisory committee meeting is an important step in the process of readying boosters for the fall and winter season, but ...
Vinay Prasad's Appointment To FDA's CBER Triggers Questions Over Future Of Cell And Gene Therapy Regulation
FDA names Vinay Prasad to lead CBER, raising questions over biologics oversight and triggering biotech stock losses and ...
Chiang Rai Times23h
FDA Commissioner Marty Makary Appoints Vinay Prasad to Lead CBER.
(CTN News) – The Food and Drug Administration (FDA) has elected to appoint a new director for the Center for Biologics ...
pharmaphorum18h
FDA fast-tracks Sanofi's experimental chlamydia vaccine
The French pharma group has just been granted a fast-track designation from the FDA for a preclinical-stage mRNA-based vaccine candidate that is due to start a phase 1/2 trial in the coming days ...