FDA will let US trials of AstraZeneca and Oxford’s coronavirus vaccine resume – as reports emerge that it WORKS FDA regulators said on Friday that AstraZeneca can resume
WEDNESDAY, Oct. 7, 2020 — Eli Lilly and Co. is seeking U.S. approval for emergency use of an experimental antibody therapy for COVID-19. The request to the U.S.
The U.S. Food and Drug Administration has granted approval for Farxiga (dapagliflozin) oral tablets to treat adults with heart failure with reduced ejection fraction, the agency announced Tuesday.
BREAKING NEWS: FDA has APPROVED experimental drug Remdesivir for emergency use for coronavirus patients, Donald Trump reveals, days after study showed it may help the worst-hit President Donald
The U.S. Food and Drug Administration approved a clinical trial Friday that will allow Johns Hopkins University researchers to test a therapy for COVID-19 that uses plasma from
Promotional vaping Instagram posts outnumber anti-vaping content 10,000 to 1, according to a new study published in Frontiers in Communication. Despite “The Real Cost” awareness campaign launched by
This morning the FDA released two guidance documents relating to the regulation of various digital health software devices. The first is a draft guidance outlining categories of clinical decision support
(HealthDay)—Vinpocetine, a compound found in many dietary supplements, may pose a risk to women of childbearing age, U.S. health officials warn. A review by the U.S. Food and
(HealthDay)—The Synovasure Lateral Flow Test Kit was granted approval for marketing as an aid in detecting periprosthetic joint infection when evaluating patients for revision surgery, the U.S. Food
Ambien and other prescription sleep medications are getting a new "black box" warning label from the U.S. Food and Drug Association (FDA). This type of label is the
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