facility visits are outdated

The traditional, facility-based approach to specimen
collection is resource-heavy and inconvenient.

  • Negative experiences due to discomfort and inconvenience
  • Expensive cold-chain shipping and challenging logistics
  • Limited diversity & recruitment due to onsite collection
  • Not ideal for very young participants, or the elderly

discover modern, specimen collection

Mitra® devices with VAMS®  technology, facilitate more convenient and accurate remote sampling.

  • Enables precise, user-friendly specimen collection
  • Suits high throughput sample processing
  • Overcomes challenges of filter paper, urine cups, spit tubes, etc.
  • Comes in four formats for a variety of use cases
Mitra cartridge format standard with bar codes and specimen bag.

The Mitra® Cartridge

This user-friendly, trackable format is best suited for remote sampling that can be performed by anyone, anywhere. 

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custom-home-remote-collection-kit_extrasupercrop-3

The Mitra® Collection Kit

Convenient solution that includes all the essentials for remote sampling from home, storage and transportation. 

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Mitra Clamshell original format, research and method development

The Mitra® Clamshell

This basic format is an easy way to start experimenting with VAMS® technology.

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Processing and analyzing dried blood samples with the Mitra 96 autorack is easy since they are compatible with existing liquid handlers

The Mitra® 96-Autorack

Designed for high throughput Mitra® microsample processing including plate building and high throughput extractions. Available empty or fully loaded with 96 microsamplers.

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Still exploring or have questions about microsampling?

We’re happy to help, so please reach out!

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Mitra devices are intended as a specimen collector and for the storage and transport of biological fluids. They are CE-IVD self-certified in the UK and EU, a Class 1 IVD in Australia, and registered with Health Canada. In the United States, Mitra devices are for Research Use Only (RUO). In some countries, Mitra devices may be used in clinical diagnostic laboratory systems after the laboratory has validated their complete system in compliance with relevant rules and regulations. 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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