Typhoid Igg/Igm Rapid Test Kits Suppliers & Bulk Manufacturers
Available Forms: Cassette-based immunochromatographic test kits/Dipstick or strip formats
Available Strengths: sensitivity typically over 90%
Reference Brands: AccuQuik, J. Mitra, and Biogenix(US)
Category:
Rapid Test Kits
Typhoid IgG/IgM rapid test kits detect specific antibodies produced during infection, providing quick diagnosis of recent or past typhoid fever. They offer results within 15-20 minutes, enabling timely treatment, reducing transmission, and supporting effective outbreak control, especially in resource-limited or remote settings.
Typhoid IgG/IgM Rapid Test Kits is available in Cassette-based immunochromatographic test kits/Dipstick or strip formats
and strengths such as sensitivity typically over 90%.
Sourced from GMP-certified and ISO-compliant manufacturers, this API meets
global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical
formulation and commercial manufacturing, Typhoid IgG/IgM Rapid Test Kits is supplied in
bulk quantities with complete regulatory support including DMF, COA, and MSDS.
|
Technical Specifications & Supply Details
|
| Lead Time |
7 to 60 days (depending on batch size & schedule) |
| MOQ |
As per manufacturer’s batch size |
| COA |
Available with every batch |
| Regulatory Dossier / DMF |
Available upon request |
| Export Documentation |
FSC, COA, Manufacturing License, Product Permission |
| Standards |
IP, BP, USP |
| Certifications |
WHO-GMP, EU-GMP, USFDA (as applicable) |
Typhoid IgG/IgM Rapid Test Kits can be exported to over 30 countries across Asia, Africa, Europe,
and Latin America. Flexible packaging, competitive pricing, and a verified supplier
network make Pharmatradz a trusted sourcing partner for pharmaceutical companies
and contract manufacturers worldwide.
Product Description:
Typhoid IgG/IgM Rapid Test Kits are approved in both the US and EU, supported by dossiers demonstrating high sensitivity, specificity, and manufacturing quality. In the US, FDA clearance is required, while in the EU, CE marking certifies compliance with in vitro diagnostic regulations. These kits undergo rigorous validation, clinical performance testing, stability assessments, and quality audits. Proper documentation includes safety profiles, performance data, and certification details. To access comprehensive licensing information, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Stay informed on global regulatory standards to ensure reliable typhoid testing solutions for effective outbreak management and disease control.
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