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Updated : 7 months, 3 weeks ago IST
New Delhi [India], April 15 (ANI): In view of the rapid surge in coronavirus cases in India, the Central government approved a significant streamlining and fast-tracking of the regulatory system for COVID-19 vaccines approved for restricted use by US FDA, EMA, UK MHRA, PMDA Japan or which ar
New Delhi [India], April 15 (ANI): The Central Government on Thursday issued the regulatory pathway in India for COVID-19 vaccines approved for restricted use by US FDA, EMA, UK MHRA, PMDA Japan or which are listed in WHO Emergency Use Listing (EUL), said the Union Health Ministry.
Updated : 7 months, 4 weeks ago IST
Johannesburg [South Africa], April 14 (ANI): South African Health Minister Zweli Mkhize on Tuesday said that the country will be suspending the use of the Johnson & Johnson COVID-19 vaccine after health concerns raised by the US Food and Drug Administration (FDA).
Washington [US], April 13 (ANI): The US Centers of Disease Control and Prevention (CDC) and the US Food and Drug Administration (FDA) have recommended "pause" in the use of Johnson and Johnson COVID-19 vaccine "out of an abundance of caution" over six reported cases in the US of a "rare and
Updated : 8 months ago IST
New York [US], April 10 (ANI): Pfizer and BioNTech requested the US Food and Drug Administration (FDA) on Friday for an amendment to its emergency use authorization of its Covid-19 vaccine, to expand its use for children ages 12 to 15 in the United States.
Updated : 8 months, 1 week ago IST
Washington [US], April 6, (ANI): The United States will still have enough vaccines for all Americans by the end of next month, despite problems with a single batch of "drug product" resulting in the loss of 15 million doses of Johnson & Johnson's vaccine, the White House said on Monday.
Washington [US], April 2 (ANI): Johnson and Johnson (J&J) vaccine supplier Emergent BioSolutions said in a statement that it acknowledges it botched a batch of vaccines but is confident of its ability to meet US government safety requirements and standards.
Updated : 8 months, 2 weeks ago IST
Washington [US], March 27 (ANI): The American multinational technology company, Amazon has received Food and Drug Administration authorization (FDA) for its COVID-19 test developed by its subsidiary STS Lab Holdco and the company is now intending to utilize it for its employee testing progra
Mumbai (Maharashtra) [India], March 24 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval from the United States Food & Drug Administration (US FDA) for Chlorpromazine Hydrochloride Tablets USP, 10 mg, 25 mg, 50 mg, 100 mg, and 200 mg, the generic v
Mumbai (Maharashtra) [India], March 23 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Diltiazem Hydrochloride Extended-Release Capsules USP, 60 mg, 90 mg, and 120 mg, the generic ver
Updated : 8 months, 3 weeks ago IST
Washington [US], March 17 (ANI/Sputnik): The US government issued simplified rules for developers of coronavirus tests to promote serial screening, a process in which the same individual is tested multiple times within a few days, the Food and Drug Administration (FDA) said.
Updated : 9 months ago IST
Mumbai (Maharashtra) [India], March 11 (ANI): The Maharashtra Food and Drugs Administration (FDA) on Thursday said it is working to bring down the cost of the Remdesivir 100 mg injection, used for treating critical COVID-19 patients.