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Mar 28, 2020 · On Thursday, the FDA amended their emergency policy around diagnostic testing for SARS CoV 2, the novel coronavirus that causes COVID 19. Following on a change made March 16, the agency opened the door for a number of specific private entities and labs to develop and distribute tests that can provide results on the spot in as little as 15 minutes but there are some pretty big caveats 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 National Health Laboratory ServiceResearch conducted covers a wide spectrum of activities in the pathology and surveillance disciplines. The research agenda covers the priority diseases within South Africa, such as HIV and AIDS, tuberculosis, malaria, pneumococcal infections, occupational health, screening for cervical cancer and malnutrition. Read
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