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SILVER SPRING, Md., June 16, 2020 /PRNewswire/ Today, the U.S. Food and Drug Administration revoked the emergency use authorization (EUA) of the Chembio Diagnostic System, Inc. (Chembio) DPP COVID 19 IgM/IgG System, a SARS CoV 2 antibody test, due to performance concerns with the accuracy of the test.CategoryPress Release Smart Industry NewsWith this new approval, KEYTRUDA is now approved for five indications across three different types of cancer in China, including as a first line treatment for appropriate patients with advanced non small cell lung cancer (monotherapy and in combination with chemotherapy) and as a second line treatment for advanced melanoma. The U.S. Food and Drug Administration approval in July 2019 was based Fimea publishes information on granted exemptions starting <p>The Finnish Medicines Agency Fimea has prohibited Testerit.fi/Global Network Oy from selling, marketing, and distributing the 2019 nCoV IgG/IgM Rapid Test Cassette Single use kit coronavirus test on 29 April 2020. The ban is effective immediately, and it will last until 31 August 2020.

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