the microsampling blog / home blood collection

In some territories, which are listed in our website footer, our microsampling devices are supplied for therapeutic or IVD use as referenced in some of our content. Outside of those territories our devices are supplied for research use only (RUO).

methotrexate TDM using whole blood microsamples

by James Rudge, PhD, Technical Director, Neoteryx | 5 min read

methotrexate TDM using whole blood microsamples

An article by Dala N. Daraghmeh et al in Australia, published in the July 2022 issue of Analytical and Bioanalytical Chemistry, reported on an investigation into relative levels of methotrexate …

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VAMS for monitoring tyrosine kinase inhibitors

by James Rudge, PhD, Technical Director, Neoteryx | 3 min read

VAMS for monitoring tyrosine kinase inhibitors

An article published by Nick Verougstraete and Christophe P. Stove in the January 2022 issue of the Journal of Pharmaceutical and Biomedical Analysis, demonstrated a robust analytical validation of eight …

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microsampling to differentiate type 1 vs type 2 diabetes

by James Rudge, PhD, Technical Director, Neoteryx | 6 min read

microsampling to differentiate type 1 vs type 2 diabetes

An article published in the March 2018 issue of the Journal of Diabetes Science and Technology, reported on the use of blood microsamples to measure C-peptide as a biomarker for …

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Mitra® devices are intended as a specimen collector and for the storage and transport of blood. They are CE-IVD in the UK and EU, a Class 1 IVD in Australia, Brazil & China, Class B in South Africa, and registered with health agencies in Canada and Ukraine. 

In the USA, Mitra devices are supplied as a Research-Use Only (RUO) product, to assist in method development, other research-related and non-diagnostic activities. Mitra has not been validated for use with any diagnostic testing. The suitability of Mitra for any analytical application must be evaluated and validated by the laboratory or research institute in a manner consistent with local regulatory requirements. 

hemaPEN® is supplied for therapeutic or IVD use in Australia, New Zealand, UK, EU and USA only: ARTG number: 280007; CE mark, general IVD; US FDA number: D410490. Outside of the territories listed above, the hemaPEN is supplied for research use only (RUO) and not for therapeutic or diagnostic use. 

Mitra®, VAMS® & hemaPEN® are registered trademarks owned by Trajan Scientific Australia Pty Ltd. 

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