Urine Drug Test Panels (Single/Multi-Panel) Suppliers & Bulk Manufacturers
Available Forms: Dipstick/Strip Tests/Cassette-based panels/Cup/Specimen collection kits
Available Strengths: Sensitivities around 50-100 ng/mL
Reference Brands: Quest Diagnostics, Abbott iScreen, Clinitek, Acer, PharmaScreen(US)
Category:
Rapid Test Kits
Urine drug test panels detect specific drugs or drug classes by identifying metabolites through immunoassay techniques. They offer quick, reliable results within minutes, supporting early diagnosis, treatment planning, and drug screening in healthcare, workplace, and law enforcement settings. Benefits include non-invasive testing, high accuracy, and rapid turnaround times.
Urine Drug Test Panels (Single/Multi-panel) is available in Dipstick/Strip Tests/Cassette-based panels/Cup/Specimen collection kits
and strengths such as Sensitivities around 50-100 ng/mL.
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, Urine Drug Test Panels (Single/Multi-panel) 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) |
Urine Drug Test Panels (Single/Multi-panel) 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:
Urine drug test panels, both single and multi-panel, are approved in the US and EU, supported by dossiers demonstrating high sensitivity, specificity, and manufacturing quality. In the US, FDA clearance regulates these tests, while CE marking ensures compliance with IVDR standards in the EU. Rigorous validation, clinical performance testing, stability assessments, and quality audits are conducted prior to approval. 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 drug testing solutions essential for clinical, workplace, and legal applications worldwide.
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