Human Albumin

Name: Human Albumin
Brand: Artemisine Medicines Technology Co., Ltd.

Injection

Human Albumin — GMP manufactured injection by Artemisine Medicines Technology. Original manufacturer supply with stable quality, factory direct price and full batch documentation for global markets.

Product Name	Human Albumin
Dosage Form	Injection
Strength	20%
Standards	BP / ENTERPRISE
Packing	Customized per market requirement (bottle / blister / box)
Documents	COA, COPP, DMF, CTD Dossiers
MOQ	Contact us for MOQ and current stock

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WHO Prescribing Guidance

Indications · Administration · Dosage · Precautions

Reference information summarised from WHO prescribing guidance. Expand each item below — clinical use must always follow the locally approved product insert.

🎯Indications▾

Hypovolaemia and shock where crystalloids are insufficient, severe hypoalbuminaemia, large-volume paracentesis in cirrhosis and burns (as per national protocol).

💧Administration▾

Intravenous infusion only, using an appropriate filter; inspect for turbidity before use.

⚖️Dosage▾

Adults 20% solution typically 100–200 ml per infusion; 5% solution 250–500 ml, adjusted to the clinical response and haemodynamic parameters. Hospital use only.

⚠️Precautions & Warnings▾

Avoid in patients with cardiac failure or pulmonary oedema risk (fluid overload), severe anaemia and known albumin hypersensitivity. Monitor blood pressure, pulse and urine output during infusion.

Reference: WHO Model Formulary / WHO Model List of Essential Medicines. For professional reference only — clinical use must follow the locally approved product insert and national treatment guidelines.

Why Order From Us

Factory Direct. Fully Documented.

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GMP Quality

Full batch testing and quality traceability under standard GMP workshops.

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Fast Delivery

Sufficient stock on regular items, familiar with export logistics to 50+ countries.

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Registration Support

COA, DMF, dossier and legalization documents for your market registration.

FAQ

Human Albumin — Frequently Asked Questions

Which documents are provided for Human Albumin registration?

Every batch of Human Albumin ships with a Certificate of Analysis (COA). For market registration we provide COPP, DMF and CTD-format dossiers, plus legalisation support where your authority requires it.

What is the MOQ and lead time for Human Albumin?

MOQ and lead time for Human Albumin depend on strength, packaging and destination market. Send us your target market and annual volume — our export team confirms current stock, MOQ and lead time within 24 hours.

Do you support OEM / private label?

Yes. We offer OEM packaging and private-label production for Human Albumin, subject to the regulatory requirements of the destination market.

Which markets have you exported injection products to?

We have supplied injection products to 50+ countries across Africa, Southeast Asia, Latin America and the Middle East, with experience in ministry-of-health registration and international tenders.

How is the quality of Human Albumin controlled?

Human Albumin is produced in China-GMP workshops (site re-inspected and passed in 2026), released only after full QC testing against BP / enterprise standards, with retained samples kept for one year beyond the product's expiry date.

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