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the microsampling blog
Christa Nuber

Christa Nuber

Recent Posts by Christa Nuber:

what is the shelf life of blood and journey of a blood sample?

by Christa Nuber | 5 min read

what is the shelf life of blood and journey of a blood sample?

Once a blood sample has been collected and labeled, it must be delivered, shipped or otherwise transported to a lab for testing. What is the shelf life of blood samples? …

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Topics:labsDried blood testingWet blood testing

why are antibodies critical in our battle against COVID-19?

by Christa Nuber | 7 min read

why are antibodies critical in our battle against COVID-19?

Production of antibodies are part of the body's defense mechanism. They help our immune systems fight off contagious disease and reinfection. This is the concept behind vaccinations. A vaccination, such …

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Topics:Remote Blood CollectionCoronavirus

hydroxychloroquine to treat COVID-19: at-home blood collection examined

by Christa Nuber | 4 min read

hydroxychloroquine to treat COVID-19: at-home blood collection examined

At the beginning of April 2020, it was reported by Johns Hopkins University that the number of COVID-19 infections had surpassed the 1 million mark globally, and the number of …

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Topics:Remote Blood CollectionCoronavirusViral Pathogens
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The Mitra Device is a single-use, non-sterile device used as a specimen collector and for the storage and transport of blood or other biological fluids. It is designed to be used by laboratory and healthcare professionals, or end-users as a container to collect and transport blood or other biological fluids. It is not specific to any clinical test, and is not for use in diagnostic procedures. Use of the Mitra Microsampler in Laboratory Developed Tests (LDTs) requires further processing including the establishment of performance characteristics and successful validation by the laboratory in a manner consistent with CLIA and/or other regulatory requirements.
The Mitra Microsampling Device is a FDA listed Class 1 exempt device, CE-IVD self-certified in the UK and EU, a Class I IVD in Australia, and registered with Health Canada. Neoteryx operates a Quality Management System (QMS) that is based on FDA good manufacturing practices, 21 CFR 820 regulations, and ISO-13485.
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