Urine Drug Test Panels (Single/Multi-panel) bulk supplier for pharma manufacturers

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 (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.

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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.

Frequently Asked Questions

Yes, Urine Drug Test Panels (Single/Multi-panel) 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, Urine Drug Test Panels (Single/Multi-panel) 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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