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Podrobn popis Dne 26. ledna 2021 zprva PEI o oficilnm testu, kter Nmeck federln institut professional liva a zdravotnick prostedky (Bundesinstitut fr Arzneimittel und Medizinprodukte, Bf, Ar, M) prohlsil, e Lepu SARS-Co, V-2 Antigen Rapid Test Set splnil vechny minimln kritria pro testy antigenu provdn PEI po konzultaci s Robertem Koch-Institutem (RKI).

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V nvaznosti na pokyny zveejnilo rakousk spolkov ministerstvo kolstv, vdy a vzkumu na zatku ledna veejn pokyny pro celosttn testy COVID-2019 ve vech kolch. Vem kolm v Rakousku bude poskytnuto piblin pt milion rychlch testovacch souprav SARS-Co, V-2 Antigen (imuno-chromatografie na koloidnm zlat) (dodavatel: Beijing Lepu Medical Innovation Co., Ltd.

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Heinz Famann, Bundesminister fr Bildung, Wissenschaft und Forschung, prosazuje, aby se tohoto pravidelnho testovn na antigeny astnilo vce dt, tm bezpenj bude koln ivot pro dti a vechny ostatn. Vsledky za 15 minut 5-ti krokov protokol Stabiln, s vysokou citlivost (95,06% nebo a 98,54% ve vysoce pozitivnch vzorcch s Ct25) a specificitou (99,62%) Technologie imunochromatografie na bzi koloidnho zlata Nemocnice koly Letit Stanice veejn dopravy Hotely Korporace Testovac weby Hromadn veejn promtn.

BEIJING, Jan 12, 2021In November 2020, The European Commission (EC) released a Suggestion on using quick antigen tests for the medical diagnosis of SARS-Co, V-2 infection. Following This Piece Covers It Well , previously this January Austrian Federal Ministry of Education, Science and Research study published public assistance for national-wide COVID-2019 tests in all schools.

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China) for trainees will be offered to all schools in Austria. Heinz Famann, Bundesminister fr Bildung, Wissenschaft und Forschung, promotes that more children take part in this regular antigen testing, the more secure the school life becomes for kids and everyone else. As the case number of SARS-Co, V-2 infections continues to increase, tests require boosts as well: Member State's health systems and medical laboratories are under pressure and testing capabilities are typically surpassed.

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Test Uniqueness: (Medical Trial)This product is already being offered throughout Europe, consisting of Germany, Italy, Austria and other countries with substantial sales in South America and Russia.

The EU Health Security Committee has settled on a of COVID-19 fast antigen tests, a selection of quick antigen tests for which Member States will equally identify their results, and a common standardised set of information to be included in COVID-19 test result certificates. These 3 deliverables, agreed by Member States and as required by the Council Recommendation of 21 January on a typical structure for the usage of quick antigen tests, will be continually evaluated and updated.

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If negative COVID-19 tests are to be required or advised for any activity, it is vital that they are equally recognised and lead to certificates recognised throughout the EU. This is essential, particularly in the context of travel. Our people need clearness and predictability." The Joint Research Study Centre (JRC) is presently in the procedure of upgrading its COVID-19 in vitro diagnostic medical devices database, with the goal of integrating all the info on rapid antigen tests that was collected and settled on by the Health Security Committee.

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