A high-tech biotechnology company focused on R&D and production of antigens, antibodies, and downstream detection reagents for diagnosis and therapy — from raw materials to finished products.
Ningbo Medvok Medical Co., Ltd. is a high-tech biotechnology company focused on the R&D and production of antigens, antibodies and downstream detection reagents for diagnosis and therapy. The product pipelines cover cardiovascular and cerebrovascular, inflammation, infectious diseases, tumors, hormones and other categories, from raw materials to finished products.
Innovation is in our DNA! Bioantibody keeps developing new technologies. Currently, our products have been delivered to more than 60 countries and cities worldwide. Using the ISO 13485 management system, the product quality is greatly trusted by customers.
With the mission "Biotech For A Better Life", we are committed to innovation and providing our best solutions to our customers. We sincerely believe we could make our special contribution to human ecology and health.
Comprehensive IVD solutions spanning six major diagnostic categories — from upstream raw materials to finished diagnostic reagents.
High-sensitivity biomarkers including cTnI, BNP, D-Dimer, CK-MB and more for rapid cardiac risk assessment and stroke prevention diagnostics.
CRP, PCT, IL-6 and SAA reagents enabling precise inflammatory response monitoring for critical care, sepsis screening and chronic disease management.
Antigens and antibodies for HIV, HBV, HCV, influenza, COVID-19 and emerging pathogens — supporting global pandemic preparedness.
AFP, CEA, PSA, CA125, CA19-9 and a broad oncology panel for early cancer screening, staging and therapeutic monitoring applications.
TSH, T3, T4, FSH, LH, HCG, testosterone and estrogen assay components for reproductive health, thyroid and metabolic disorder testing.
Vertically integrated supply: recombinant antigens, monoclonal antibodies, colloidal gold conjugates, nitrocellulose membranes and complete LFIA/ELISA kits.
Dedicated cleanroom environments for antigen expression, antibody purification and lateral flow strip assembly meeting international GMP requirements.
Equipped with protein expression systems, HPLC purification, SPR binding analysis and full immunoassay development capabilities.
Temperature-controlled warehousing and shipping solutions ensuring product integrity from factory to end-user across all 60+ served markets.
In-process and final QC testing including sensitivity, specificity, stability and cross-reactivity analysis aligned with ISO 13485 standards.
Eight compelling reasons why leading IVD manufacturers and distributors worldwide trust us as their preferred biotech partner.
Products actively distributed in 60+ countries across Europe, Americas, Asia-Pacific, Middle East and Africa.
Full quality management system certification ensuring consistent, compliant and traceable manufacturing processes.
Dedicated R&D teams continuously developing next-generation biomarkers and detection technologies ahead of market needs.
From gene synthesis to finished kit — full supply chain control means superior quality, shorter lead times and competitive pricing.
Custom formulation, private label packaging and regulatory documentation support tailored to your specific market requirements.
Technical application specialists and regulatory affairs experts available to guide your product development and market entry journey.
Environmental and social responsibility embedded in all operations — ethical sourcing, green manufacturing and community investment.
Direct factory pricing with volume discount programs, ensuring accessible biotechnology solutions for markets at all economic levels.
Our quality credentials reflect an unwavering commitment to safety, performance and regulatory compliance in every product we manufacture.
Medical devices quality management system certification covering design, development, production, installation and servicing of all diagnostic reagent products.
CE-certified products compliant with EU In Vitro Diagnostic Regulation, enabling direct market access across all 27 European Union member states.
Good Manufacturing Practice standards implemented across all production lines, ensuring batch-to-batch consistency and product safety at scale.
We offer comprehensive white-label and custom development services, empowering global IVD brands to bring high-quality diagnostics to their local markets.
Bespoke protein expression, purification and characterization for unique biomarker targets.
Full custom branding on kits, inserts, labels and outer packaging to match your brand identity.
Technical files, clinical data and registration dossiers prepared for CE, FDA, WHO PQ and local market submissions.
Sensitivity and specificity tuning, matrix optimization and stability enhancement for your target population and sample types.
Real-world examples of how Medvok Medical's biotech solutions have delivered measurable impact for healthcare systems and diagnostic companies worldwide.
Partnered with a European distributor to supply 50M+ antigen test components within 6 months, supporting national pandemic response programs across 8 EU countries.
Developed a custom hs-cTnI LFIA kit under private label for a US-based IVD company, achieving FDA 510(k) clearance and launching in 12 states within 18 months.
Supplied AFP, CEA and CA125 antibody raw materials to a Southeast Asian IVD manufacturer, enabling a cost-effective multi-cancer early detection screening program.
Trusted by IVD manufacturers, distributors and research institutions across six continents — here's what our global partners have to say.
"Medvok's antibody raw materials consistently deliver exceptional lot-to-lot reproducibility. Their technical support team is incredibly responsive and knowledgeable. A truly reliable partner for our ELISA kit development pipeline."
"We have been sourcing cardiac marker antigens from Medvok for 5 years. The quality is outstanding, delivery is always on time, and their OEM documentation support made our CE registration process seamless."
"Their infectious disease antigen portfolio is the most comprehensive we've found. Medvok helped us launch a full respiratory panel in record time. ISO 13485 certification gives us complete confidence in their quality system."
We care about protecting human health and hope all of society to have access to clean, affordable, and reliable biotechnologies.
We are committed to making high-quality diagnostic solutions accessible and affordable for healthcare systems at every economic level across all 60+ countries we serve.
Our R&D investment drives the development of next-generation biomarkers, novel detection platforms and improved assay performance year after year.
Our economic development is compatible with proper conduct in relation to ethics, society, the workplace, the environment and respect for human rights.
We think of society as a group of individuals with equal rights and opportunities. Our sustainability policy covers environmental and social matters comprehensively.
Green manufacturing processes, waste reduction programs and carbon footprint minimization across all production facilities.
Equal opportunity employment, community health education programs and support for underserved populations in accessing diagnostic testing.
Safe, inclusive and empowering work environments where every team member can grow, innovate and contribute to our shared mission.
Ethical sourcing, fair labor practices and transparent supply chain management aligned with international human rights standards.
In the evolving landscape of healthcare, in vitro diagnostic (IVD) testing has become essential. "What is in vitro diagnostic testing and how does it
Author: Aria Date: 2026-03-30
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