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Rapid Malaria PF/PV Antigen Card Test bulk supplier for pharma manufacturers

Rapid Malaria Pf/Pv Antigen Card Test Suppliers & Bulk Manufacturers

Available Forms: Test Kits

Available Strengths: 1 test/kit

Reference Brands: SD BIOLINE Malaria (USA), CareStart Malaria HRP2/pLDH (USA/EU), Meril Malaria Pf/Pv Test (India)

Category: Rapid Test Kits

Malaria Pf/Pv Antigen Rapid Test (RDT) performs as a better sensor and discriminator of malarial parasites and their species and appears to be an acceptable tool for diagnosis of malaria in symptomatic patient. Rapid Malaria PF/PV Antigen Card Test is available in Test Kits and strengths such as 1 test/kit. 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, Rapid Malaria PF/PV Antigen Card Test 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)

Rapid Malaria PF/PV Antigen Card Test 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.

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📘 Sourcing Guide

Product Description:

The ICT Malaria P.f./P.v. test is a rapid immunochromatographic assay designed for the qualitative detection of malaria infections in human blood. Manufactured in a convenient test card format, it provides quick and reliable results, making it suitable for point-of-care and field use, especially in resource-limited settings. The test specifically detects histidine-rich protein 2 (HRP2), an antigen produced by Plasmodium falciparum, along with a panmalarial antigen that is shared across multiple Plasmodium species.

This dual-detection capability allows the test to identify infections caused by both Plasmodium falciparum and Plasmodium vivax, the two most common malaria-causing parasites. Field studies have demonstrated its effectiveness in detecting P. vivax, expanding its diagnostic utility. While earlier findings suggested limitations in detecting P. malariae, emerging evidence indicates that the panmalarial antigen targeted by the test may also be expressed by this species, enhancing its potential diagnostic scope.

Overall, the ICT Malaria P.f./P.v. test serves as a valuable tool for rapid screening and early diagnosis, supporting timely treatment decisions and helping to control the spread of Malaria.

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Frequently Asked Questions

It is used for the qualitative detection of Plasmodium falciparum and Plasmodium vivax antigens in human blood to aid in the diagnosis of Malaria infection.

It is based on lateral flow immunoassay technology using specific antibodies against malaria antigens such as HRP2 and pLDH, along with nitrocellulose membrane strips and labeled conjugates for antigen detection.

It is marketed under multiple trade names such as SD BIOLINE Malaria Ag P.f/P.v, CareStart Malaria Test, First Response Malaria Ag Combo, Parascreen, and OnSite Malaria Rapid Test.

It is manufactured by multiple companies including SD Biosensor, Access Bio, Premier Medical Corporation, Zephyr Biomedicals, CTK Biotech, Nal von Minden, bioMérieux, Meril Diagnostics, J Mitra & Co., Span Diagnostics, and Tulip Diagnostics.

The generic name is Plasmodium falciparum / Plasmodium vivax (PF/PV) Antigen Rapid Diagnostic Test (Lateral Flow Immunoassay).

Common brand names include SD BIOLINE Malaria Ag P.f/P.v, CareStart Malaria HRP2/pLDH, First Response Malaria Ag Combo, and Parascreen Rapid Test.

These kits are manufactured globally across regions including the United States, European Union countries, India, China, and South Korea by various diagnostic companies.

Yes, Rapid Malaria PF/PV Antigen Card Test is available with DMF and other regulatory documents such as COA and MSDS. These can be provided upon request for qualified buyers.

Absolutely. Sample requests are accepted for formulation trials and quality checks. Please submit an enquiry to initiate the process.

Our manufacturing partners are GMP-certified and comply with ISO and WHO standards, ensuring global quality benchmarks.

Lead times vary based on quantity and destination, but most orders are fulfilled within 1–3 weeks. Express shipping options are available.

Yes, Rapid Malaria PF/PV Antigen Card Test is exported to over 30 countries across Asia, Africa, Europe, and Latin America. We support documentation for customs and regulatory clearance.

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