OUR PORTFOLIO
Diagnostic Solutions for
the World’s Most Pressing Health Needs
Rapid, accurate, and affordable point-of-care tests — manufactured to international quality standards and delivered at scale across Africa.
US Market · FDA 510(k) Cleared · CLIA-Waived
Cleared for the US. Stocked in the US. Ready to Ship.
FDA-cleared drug-of-abuse and pregnancy rapid tests, held in US stock with full regulatory documentation — built for occupational health, corrections, clinics, and distribution partners nationwide. 3–5 business day lead time.
Are You a US Sales Rep or Distributor?
Sell our FDA-cleared diagnostics from US stock, build your own territory, and earn on every reorder.
Become a Sales Rep
QUALITY & STANDARDS
Built to Global Standards
Every Ash Biomedical product is produced under a rigorous quality management framework. As the legal manufacturer of its full portfolio, Ash Biomedical’s products are produced in ISO 13485-certified, CE-marked facilities — meeting the international standard for medical device quality systems. All commercial products are registered with Nigeria’s NAFDAC and aligned with WHO prequalification guidelines.
ISO 13485
Medical Device Quality Management
NAFDAC
National Regulatory Registration
WHO
Prequalification-Aligned Protocols
CE Mark
European Medical Device Standard
Interested in Our Products?
Whether you are a government health ministry, NGO, or private healthcare distributor, we would welcome the opportunity to discuss how Ash Biomedical’s diagnostic solutions can serve your program needs.