Every microsampling success story is based on unique objectives. Your Microsampling Specialist will be with you every step of the way and help you develop a winning strategy to make the most of this transformative dried blood collection technology.
Along with personalized guidance, you'll have access to our methods and protocols, detailed case studies and resources to help you successfully develop methods for your analytes of interest. Your Microsampling Specialist will be there to address your concerns and questions, as they arise.
After you review your study data with your Microsampling Specialist, you'll define your objectives for a full bioanalytical and clinical validation. This is also the time to loop in key stakeholders. We'll see you through the challenge and triumph of implementing this smarter, simpler, blood collection technology company-wide.
You're about to take your first step toward a future of better blood collection.
When we receive your information, our experts will contact you to review your evaluation objectives and get you started in the way that makes sense for you and with the Mitra® format that meets your needs.
421 Amapola Ave
Torrance, CA 90501
Call us: 1 (310) 787-8747
info@neoteryx.com
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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