 
Where Certainty is Manufactured.
Every Tashikin diagnostic is a promise of reliability. That promise is forged in our state-of-the-art facility and powered by our proprietary NomoFlow™ platform.
We Believe Reliability Isn't a Feature. It's the Foundation.
In a world of complex biology, the quality of your diagnostic tool cannot be a variable. At Tashikin, we obsessed over perfecting the manufacturing process before we ever sold a single test. This commitment to foundational excellence is what allows you to trust the results in your hands, every single time.
The Science Inside: The NomoFlow™ Platform
NomoFlow™ is not just a process; it's our end-to-end quality and technology engine. It integrates advanced material science, automated robotics, and real-time data monitoring to create a new standard in diagnostic consistency.
Unmatched Lot-to-Lot Consistency
NomoFlow™ minimizes the human and environmental variables that cause inconsistency, ensuring the test you use today performs identically to the one you'll use next year.
Enhanced Sensitivity & Specificity
By precisely controlling the deposition of biologics and the flow dynamics of each test, we optimize the reactions that are critical for detecting subtle signs of disease.
Built-in Reliability & Stability
Our automated sealing and multi-stage drying processes create robust tests that maintain their integrity from our factory to your clinic, even in challenging conditions.
A Commitment to Transparency: Our Facility
 
1. Research & Development Core
Our journey begins in our dedicated R&D labs, where new biomarkers are validated and assay performance is relentlessly optimized before ever entering production.
 
2. Fully Automated Production
Robotics and machine vision guide every step of assembly, from precision reagent jetting to final cassette sealing, ensuring unparalleled uniformity.
 
3. Multi-Stage Quality Control
Beyond visual inspection, every batch is functionally challenged against a library of standards in our QC lab. No product ships without passing our rigorous performance criteria.
Certified to a Higher Standard
ISO 13485:2016
This certification affirms that our quality management system meets the stringent global standard for medical device manufacturing, covering everything from design to distribution.
Current Good Manufacturing Practices (cGMP)
We operate in compliance with cGMP regulations, ensuring our facility, processes, and controls are robustly designed for safety, identity, strength, quality, and purity.
The Result? Confidence in Your Hands.
Our manufacturing excellence isn't for us—it's for you. It's the reason you can be certain about the diagnosis, certain about your treatment plan, and certain about the care you provide.
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