CENTOGENE Receives FDA Emergency Use Authorization for COVID-19 Molecular Diagnostic Test
Centogene N.V. - Common Shares (CNTG)
Last centogene n.v. - common shares earnings: 12/5 06:28 am
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Source: GlobeNewswire
CAMBRIDGE, Mass. and ROSTOCK, Germany and BERLIN, July 02, 2020 (GLOBE NEWSWIRE) -- Centogene N.V. (Nasdaq: CNTG), a commercial-stage company focused on rare diseases that transforms real-world clinical and genetic data into actionable information for patients, physicians, and pharmaceutical companies, today announced that the U.S. Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for the company's SARS-CoV-2 RT-PCR test. Prof. Arndt Rolfs, CEO of CENTOGENE, said, “Over the past several months, we have been working tirelessly to ensure that we provide the best possible molecular diagnostic testing to prevent the further outbreak of COVID-19 and support the return to a new normal. This authorization by the FDA is another milestone for our COVID-19 testing efforts that validates the quality, precision and reliability of our tests.” “CENTOGENE is proud to have received this accelerated authorization from the FDA, which recognizes our continued commitment
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CNTG
Sec Filings
- 4/2/24 - Form 6-K
- 3/19/24 - Form 6-K
- 2/29/24 - Form 6-K
- CNTG's page on the SEC website