FDA Authorizes Quest Diagnostics’ Proprietary Monkeypox Test for Emergency Use

    0
    144

    First lab-developed test specifically designed to detect Monkeypox virus DNA to receive emergency use authorization during the monkeypox public health emergency SECAUCUS, N.J., Sept. 7, 2022 /PRNewswire/ — Quest Diagnostics (NYSE: DGX), the world’s leading provider of diagnostic…

    Advertisment
    Previous articleThe Economist’s midterm election model shows Republicans have a 74% chance of winning the House …
    Next articleMatternet M2 Drone Delivery System First to Achieve FAA Type Certification

    LEAVE A REPLY

    Please enter your comment!
    Please enter your name here