evelopments relating to federal legalization: (1) the U.S. Food and Drug Administration (FDA) will begin approving individual pharmaceuti

ion Farm Bill Agricultural Act of 2014 FDA U.S. Food and Drug Administration, an agency of the DHHS FD&C Act Federal Food, Dru

streamlined. Some of the most significant improvements have been in therapeutic areas where there is a high level of unmet medical need. For example, the U.S. Food and Drug Administration (“FDA”) is demonstrating clear interest in working more constructively with industry to bring new safe and effective therapeutics to market that targ

emale Health Company manufactures, markets and sells the FC2 Female Condom. FC2 is the only currently available female-controlled product approved by the U.S. Food and Drug Administration (FDA) and cleared by the World Health Organization (WHO) for purchase by U.N. agencies that provides dual protection against unintended pregnancy and

tions, Senate", "Cancer", "Celgene Corporation", "Food and Drug Administration", "Senate", "Hugin, Robert J", "New Jersey", "Men

'm writing to update you on our conversation with the U.S. Food and Drug Administration and how it impacts you. If you are a customer w

nformation took another exciting step in January. The U.S. Food and Drug Administration cleared the way for us to provide a new Genetic H

no conflict because Innate had no business before U.S. regulators. But in 2017, the company practically beamed that it had "received clearance from the U.S. Food and Drug Administration for the Company's Investigational New Drug (IND) application lodged last month." The fact that Collins' role in the legislation could also have ben

n announced additional sanctions against certain Iranian and related entities. Read more » Drug, Device Makers Cheer As FDA Punts Off-Label Policy The U.S. Food and Drug Administration on Friday once again delayed a controversial new policy related to off-label promotion, drawing cheers from drug and device makers that have decrie

n Agency FAA Federal Aviation Administration FDA Food and Drug Administration HHS Dept. of Health & Human Services HUD Dept. o

coronavirus pandemic, finding the issue should be addressed at the trial court level first. FDA Slaps Tighter Controls On COVID-19 Antibody Tests The U.S. Food and Drug Administration announced Monday that commercial manufacturers of antibody tests for COVID-19 will now be required to submit emergency use authorization requests,