Monobind Inc
Monobind enhances health in communities worldwide by supplying laboratory diagnostics which are innovative, simple to use, cost effective and vital for human-care. The company`s AccuBind ELISA and AccuLite CLIA systems are offered in the IVD areas of Thyroid, Fertility & Steroid, Tumor & Cardiac Markers, Anemia, Bone Metabolism, Diabetes, Neonatal & Prenatal, Allergy, and Infectious Disease Testing. And with VAST products, users receive a panel of markers in just one kit. Based on a 96-well microplate, Monobind kits can be run manually or with fully automated analyzers, including Monobind-brand equipment for optimal performance. In addition to diagnostic systems, Monobind processes biomaterials for the largest IVD manufacturers, providing reagent-grade fractionated human blood-products (Albumin and Gamma-Globulin), purified-human plasma, serum and urine for unique applications and exact specifications.
Company details
Find locations served, office locations
- Business Type:
- Manufacturer
- Industry Type:
- Medical Equipment
- Market Focus:
- Globally (various continents)
- Year Founded:
- 1978
About Us
Sophisticated GMP, Regulatory, and QA Commitments are the backbone to Monobind’s reliable and reproducible product line as demonstrated by our ISO 13485 Certification, CE Mark, GMP & FDA Registration and numerous Vendor Approvals and Awards from our elite customers.
A global leader in the IVD space, established in 1978, for further details see Monobind's Fact Sheet
Who We Are
Monobind Inc. is a pioneer in IVD design and production. We are a global force in 100+ countries. Our AccuBind® ELISA and AccuLite® CLIA kits have a test menu of 55+ analytes, one of most comprehensive in open-system reagents. With a strong R&D focus and manufacturing excellence, Monobind consistently delivers high-quality products. Discover why our customers choose Monobind reagents, instruments and biological materials for their most essential operations.
Quality Policy
Monobind, Inc. is committed to:
• Satisfy our Customers with high-quality, defect-free, on-time products that provide demonstrable value in the market including user-advantages, cost-benefits and availability of vital healthcare.
• Comply with all statutory and regulatory requirements.
• Continual improvements in its Quality Management System through a management review process to establish and maintain Quality Objective and System Effectiveness.
• Communicate the Quality Policy of our Company Staff to ensure understanding, participation, and a responsibility to apply the Quality Objectives in the performance of their tasks.