by James Rudge, PhD, Technical Director, Neoteryx | 5 min read
An article published in the September 2021 issue of the Journal of Pharmaceutical and Biomedical Analysis, reported on the use of dried urine samples for the measurement of banned peptide hormones in athletes. The paper, …
Read Storyby Neoteryx | 3 min read
Urinalysis has long been a staple sampling approach in toxicology research and drug screening, but conventional urine sample collection leaves much to be desired. The ‘pee-in-a-cup’ method is not only …
Read Storyby Neoteryx | 3 min read
Urinalysis is used in lab testing to detect disease and manage various health conditions. These include liver disease, kidney disease, diabetes and UTIs (urinary tract infections). Some employers also request …
Read StoryLearn about insights, research, case studies, and tutorials on integrating remote specimen collection, microsampling, and more!
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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, Brazil & China, Class B in South Africa, and registered with health agencies in Canada, Thailand, and Ukraine. 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. Mitra is a registered trademark of Neoteryx, LLC.
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. hemaPEN® is a registered trademark owned by Trajan Scientific Australia Pty Ltd.
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