Product Portfolio
Biotest HSA 20%
200 g/L · 100 mL vial
- Sterile solution
- Human plasma-derived albumin
- Pharmaceutical grade (Ph. Eur.)
- For further manufacturing and research use
- Use as Ancillary Material according to USP <1043>
Biotest HSA 5%
50 g/L · 250 mL vial
- Sterile solution
- Human plasma-derived albumin
- Pharmaceutical grade (Ph. Eur.)
- For further manufacturing and research use
- Use as Ancillary Material according to USP <1043>
Product Comparison
| Attribute |
Biotest HSA 20% |
Biotest HSA 5% |
|
Albumin concentration |
200 g/L |
50 g/L |
|
Fill volume |
100 mL |
250 mL |
|
Dosage form |
Sterile solution |
Sterile solution |
|
Origin |
Human plasma |
Human plasma |
|
Quality positioning |
Pharmaceutical grade |
Pharmaceutical grade |
|
Manufacturing |
GMP, Germany |
GMP, Germany |
|
Intended use |
Further manufacturing and research use |
Further manufacturing and research use |
Multi-compendial product information
Biotest HSA is manufactured in compliance with European Pharmacopoeia requirements for licensed drugs. Product information also addresses USP-NF <1043> on ancillary materials and relevant USP requirements for human albumin.
European Pharmacopoeia
Human Albumin Solution, monograph 0255
USP-NF <1043>
Ancillary material information; Biotest HSA is positioned as Tier 1
USP / 21 CFR 640.80–83
Human albumin product requirements
