Anagram & Information om | Engelska ordet EUA

Exempel på hur man kan använda EUA i en mening

• The ESU, EUA, EURASHE, EI, ENQA, UNICE, the Council of Europe and UNESCO are part of the process' follow-up.
• In March 2020, Abbott received emergency use authorization (EUA) from the US FDA for a SARS-CoV-2 test during the COVID-19 pandemic.
• Dmitry Albertovich Tayursky, Rector of the university, was suspended by the European University Association (EUA) following support for the 2022 Russian invasion of Ukraine by the Russian Union of Rectors (RUR) in March 2022, for being "diametrically opposed to the European values that they committed to when joining EUA".
• In March 2022, the EUA suspended 12 Russian members following the 2022 address of the Russian Union of Rectors (RUR) supporting the 2022 Russian invasion of Ukraine, for being "diametrically opposed to the European values that they committed to when joining EUA".
• To cover emissions on an ever-tightening ration of free EUA allowances, a coal-fired powered power plant will either have to abate internally or buy credits.
• ENQA worked with the other "E4" agencies, the European University Association (EUA), the European Association of Institutions in Higher Education (EURASHE) and the European Students Union (ESU), to establish the European Quality Assurance Register for Higher Education (EQAR), which makes available a validated list of higher education quality assurance agencies which adhere to the ESG, and reduces the risk of bodies which purport to grant accreditation without rigorous review.
• The all-time results of German athletes are thus divided among the designations GER, EUA, FRG, GDR and SAA (the Saarland, which only took part in the 1952 Summer Games and won no medals).
• Since the creation of Kyoto is subject to a lengthy process of registration and certification by the UNFCCC, and the projects themselves require several years to develop, this market is at this point largely a forward market where purchases are made at a discount to their equivalent currency, the EUA, and are almost always subject to certification and delivery (although up-front payments are sometimes made).
• EEX currently runs a secondary market for continuous trading on a spot and derivatives basis for EU ETS allowances (EUA, EUAA) and Kyoto credits (CER, ERU).
• German lugers (competing under the IOC country codes of EUA, GDR, FRG and GER at different times since 1964) have dominated the competition, winning 87 medals of 153 possible.
• The data supporting the US Food and Drug Administration (FDA) emergency use authorization (EUA) for baricitinib combined with remdesivir was based on a randomized, double-blind, placebo-controlled clinical trial (ACTT-2), which was conducted by the US National Institute of Allergy and Infectious Diseases (NIAID).
• After clinical trials, in December 2021, the oral medication nirmatrelvir (formerly PF-07321332) became commercially available under emergency use authorizations (EUA), as part of the nirmatrelvir/ritonavir combination therapy (brand name Paxlovid).
• Efforts included development of an EUA (Expanded Access Authorized) laboratory-based PCR test, development of serologic assays for SARS-CoV-2 (the virus that causes COVID-19), analysis of persistence and decay of human antibody responses in COVID-19 patients, assessment of test performance characteristics of available serological and PCR assays against SARS-CoV-2, development of ultrasensitive antigen and antibody detection systems for SARS-CoV-2, assessment of immunologic cross-reactivity of SARS-CoV-2 with other coronaviridae, assessment of immune responses to SARS-CoV-2 in children, assessment of COVID-19 in Bangladesh, analysis of antibody functionality and signature during SARS-CoV-2 infection in relationship to mortality outcome, comparison of immune responses following vaccination to those induced by SARS-CoV-2 infection, assessment of plasma viral load with severity and mortality, and evaluation of the genomic epidemiology of SARS-CoV-2 in the Boston area.
• In November 2020, the FDA issued an emergency use authorization (EUA) for the combination of baricitinib with remdesivir, for the treatment of suspected or laboratory confirmed COVID19 in hospitalized people two years of age or older requiring supplemental oxygen, invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO).
• The FDA issued an emergency use authorization (EUA) for the combination of baricitinib with remdesivir, for the treatment of suspected or laboratory confirmed COVID-19 in hospitalized people two years of age or older requiring supplemental oxygen, invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO).
• COVID-19 drug development: The FDA issues an emergency use authorization (EUA) for bamlanivimab and etesevimab.
• University of Minnesota professor David Boulware, who filed the EUA application, said that the standard that they were holding for fluvoxamine was a different standard than the other big pharma trials, with Paxlovid and molnupiravir and the monoclonals.
• The data supporting the emergency use authorization (EUA) for bamlanivimab and etesevimab are based on a randomized, double-blind, placebo-controlled clinical trial in 1,035 non-hospitalized participants with mild to moderate COVID-19 symptoms who were at high risk for progressing to severe COVID-19.
• In November 2020, the FDA issued an emergency use authorization (EUA) for the combination of baricitinib with remdesivir, for the treatment of suspected or laboratory confirmed COVID-19 in hospitalized people two years of age or older requiring supplemental oxygen, invasive mechanical ventilation, or extracorporeal membrane oxygenation (ECMO).

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