Raw Material

• Human Plasma from US-licensed plasma donation centers
• Donor screening and virus testing per 21 CFR 610.40
• cGMP Raw Material – Cohn Fraction V

Manufacturing

• Type II eCTD DMF (#019354) on file with FDA
• Formulated with WFI (water for injection)
• Does not contain stabilizers Caprylate or N-Acetyl-L-Tryptophanate
• No animal-derived materials are used in the manufacture of this product
• Sterile microfiltration followed by aseptic filling

Quality

• Relevant cGMP guidelines used in manufacture, testing, and release
• USP Chapter <1043>, Ancillary Materials for Cell, Gene, and Tissue-Engineered Products
• ISO 13485:2016, Medical Devices – Quality Management Systems – Requirements for Regulatory Purposes
• ISO/TS 20399-1-3:2018, Biotechnology – Ancillary Materials Present During the Production of Cellular Therapeutic Products
• High Purity, Low Endotoxin – Endotoxin, and Sterility testing per USP/EP; Mycoplasma testing per EP

Stability

• 24-month stability (vials)
• Store at 2-8 °C
• Transport with cold packs

For Use Statement

For research use or further manufacturing use in ex vivo cell therapy applications. This product is not intended for direct in vivo use or for direct clinical use as a drug, therapeutic, biologic, or medical device.

Albumin is the most abundant protein in blood plasma and has historically been used in cell culture for its ability to support mammalian cell growth. Albumin is known to carry many important substances including lipids, amino acids, hormones, peptides, metals, and other undefined low molecular weight molecules. It also offers antioxidant protection to cells and participates in the transport and signal mechanics of hormones and growth factors. Akron’s cGMP-compliant HSA 25% Solution can be used in a wide range of applications such as cell culture supplementation, assay standardization, protein stabilization, and product formulation.