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A study protocol and informed consent were initiated and approved by the Sharp Institutional Nachprüfung Board. Subjects were included if they were >18 years of age and understood the study and its requirements. Patients who had impairment of cognition or decision-making capacity were excluded. Subjects were screened by research coordinators to determine if they had a nares SARS-CoV-2 RT-PCR test result, and then consent welches requested to enroll them in the study.
“MED package XTRA†test instrument Zusammenstellung for testing the effectiveness of protective measures at stationary electrical installations after completion, repair or Aufschwung, and for periodic testing, especially for the fulfillment of DGUV regulation 3.
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The test result of rapid tests, which are on the Tücke of the European Commission for COVID-19 antigen rapid tests, is recognized rein all member states of the EU. This might also interest you:
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Days from symptom onset were captured from an electronic medical record which documented self-reported data from Leikang patients reporting on the number of days they had been sick at the time of study enrollment.
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PROFITEST – saves time and money As single test instrument for a broad Auswahl of applications All measurements without any bothersome replugging of the measurement cables Can be used all over the world thanks to language selection
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