FDA Process For COVID-19 Test
FDA has announced Emergency Use Authorization (EUA) for a 5-minute point-of-care COVID-19 test, the virus that produces the novel coronavirus, according to a press statement….
FDA has announced Emergency Use Authorization (EUA) for a 5-minute point-of-care COVID-19 test, the virus that produces the novel coronavirus, according to a press statement….
As the COVID-19 pandemic continues to extend the U.S. healthcare system and limit the number of state health care providers, APhA and other major chemistry…
The first group of combined hand sanitizers has been delivered to first responders in Southeast Texas, following federal regulators’ approval for compounding pharmacies to produce…
The U.S. Food and Drug Administration (FDA) received two crucial actions in the agency’s continuing and aggressive dedication to addressing the coronavirus outbreak (COVID19).Principally, the…
The FDA is currently delaying most international reviews through April, active immediately, due to the global COVID-19 break, one and the company is considering actions…
The U.S. Food and Drug Administration now signed Ofev (nintedanib) oral capsules to manage the sufferers with chronic fibrosing (scarring) interstitial lung diseases (ILD) with…
The U.S. Food and Drug Administration has established an application for the first generic of Daraprim (pyrimethamine) pills for the treatment of toxoplasmosis (an infection…
Esperion bempedoic acid (Nexletol) tablet has gained FDA approval for use in lowering low-density lipoprotein cholesterol (LDL-C) in adults with heterozygous familial hypercholesterolemia (HeFH) or…
The U.S. Food and Drug Administration (FDA) has accepted the first generic of ProAir HFA (albuterol sulfate) Inhalation Aerosol for the therapy or blocking of…
Now, the U.S. Food and Drug Administration took extra steps to secure a smooth regulatory change aimed at improving patient access to insulin results used…