the microsampling blog / blood samples

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).

monitoring mycotoxin exposure using VAMS

by James Rudge, PhD, Technical Director, Neoteryx | 4 min read

monitoring mycotoxin exposure using VAMS

An article published by Arnau Vidal et al at Ghent University, Belgium in the May 2021 issue of Toxins reported on a method for analysis of 24 mycotoxins found in popular …

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clinical trial: bridging between VAMS and traditional samples

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

clinical trial: bridging between VAMS and traditional samples

This blog begins with a review of an article published by David Sciberras et al at UCB Biopharma and PRA Health sciences in the January 2019 issue of Pharmacology Research …

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Using LC-MS/MS to measure mAbs from VAMS extracts

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

Using LC-MS/MS to measure mAbs from VAMS extracts

An article published by X. Gao and Y. Xu et al at Merck & Co., Inc. in the January 2021 issue of the Journal of Pharmaceutical and Biomedical Analysis demonstrated …

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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 entities in the Trajan Group. 

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