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The FDA has authorized three COVID-19 vaccines for emergency use during the pandemic: Moderna, Johnson & Johnson and Pfizer-BioNTech, the last of which has received the FDA's full stamp of ...
Medscape is a website providing access to medical information for clinicians and medical scientists; the organization also provides continuing education for physicians and other health professionals. It references medical journal articles, Continuing Medical Education (CME), a version of the National Library of Medicine 's MEDLINE database ...
Tests are generally divided into two types. Viral testing can identify if a person is currently infected with SARS-CoV-2. Antibody testing can identify if a person has previously been exposed to the virus. [64] As of August 2020, the FDA had granted Emergency Use Authorizations to over 200 tests for detecting current or past infection. [65]
An Emergency Use Authorization (EUA) in the United States is an authorization granted to the Food and Drug Administration (FDA) under sections of the Federal Food, Drug, and Cosmetic Act as added to and amended by various Acts of Congress, including by the Pandemic and All-Hazards Preparedness Reauthorization Act of 2013 (PAHPRA), as codified by 21 U.S.C. § 360bbb-3, to allow the use of a ...
The U.S. Federal Drug Administration (FDA) approved testing pooled samples to help speed up the coronavirus detection process and conserve supplies. The FDA reissued an existing emergency use ...
The program, dubbed the "Coronavirus Treatment Acceleration Program," or CTAP, will see the FDA redeploy resources and personnel with an eye toward providing private companies, researchers and ...
[209] [210] As of 26 January 2021, all air passengers ages two and older must show proof of a negative COVID-19 test to enter the United States [211] and travel restrictions were reinstated for people who visited the Schengen Area, the Federative Republic of Brazil, the United Kingdom, the Republic of Ireland and South Africa, 14 days before ...
President Donald Trump has fanned new concerns over the politicization of coronavirus vaccine approvals, suggesting he could block stricter guidance from the FDA.