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View all search resultsThe rapid pace of COVID-19 vaccine development and scant information about the US Food and Drug Administration's (FDA) vaccine review process are leading to concerns, the American Medical Association (AMA) said on Wednesday.
The US Food and Drug Administration on Monday revoked its emergency use authorization for hydroxychloroquine to treat COVID-19, but quickly came under fire from President Donald Trump, who said only US agencies have failed to grasp its benefit in fighting the coronavirus.
Novartis has won the go-ahead from the US Food and Drug Administration to conduct a randomized trial of malaria drug hydroxychloroquine against COVID-19 disease, the Swiss drugmaker said on Monday, to see if it helps patients.
The United States Food and Drug Administration has approved the first rapid coronavirus diagnostic test, with a detection time of about 45 minutes, as the country struggles to meet the demand for coronavirus testing.
US regulators approved the first medicine with an embedded sensor to help keep track of whether patients are adhering to their prescriptions, a so-called digital pill made by Otsuka Pharmaceutical Co. and Proteus Digital Health.
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