Menopause Fsh Rapid Test Kits Suppliers & Bulk Manufacturers
Available Forms: Cassette-based immunochromatographic tests/Dipstick or strip formats
Available Strengths: FSH levels typically ≥25-30 IU/L
Reference Brands: Nova Menopause Test(US)
Category:
Rapid Test Kits
Menopause FSH rapid test kits detect elevated levels of follicle-stimulating hormone (FSH) in urine, indicative of menopause. They work via immunochromatography, providing quick, reliable results within minutes. Benefits include early menopause confirmation, aiding in reproductive planning, and supporting women's health management by offering accessible, easy screening.
Menopause FSH Rapid Test Kits is available in Cassette-based immunochromatographic tests/Dipstick or strip formats
and strengths such as FSH levels typically ≥25-30 IU/L.
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, Menopause FSH 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) |
Menopause FSH 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:
Menopause FSH rapid test kits are approved in both the US and EU, supported by dossiers demonstrating high sensitivity, specificity, and manufacturing quality in accordance with GMP and IVDR regulations. In the US, FDA clearance is required, while in the EU, CE marking ensures compliance with in vitro diagnostic standards. These kits undergo rigorous validation, clinical performance testing, stability assessments, and quality audits. Proper documentation includes safety profiles, performance data, and certification details. For detailed licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Staying informed ensures reliable, compliant menopause screening solutions to support women’s health management worldwide.
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