21 CFR § 640.103 Additional Standards for Human Blood and Blood Products

§ 640.103 The final product.

Current through Sep 8, 2026 · Read all of Part 640

(a) Final solution. The final product shall be a 16.5 ±1.5 percent solution of globulin containing 0.3 molar glycine and a preservative.

(b) Protein composition. At least 96 percent of the total protein shall be immunoglobulin G (IgG), as determined by a method that has been approved for each manufacturer by the Director, Center for Biologics Evaluation and Research, Food and Drug Administration.

[38 FR 32089, Nov. 20, 1973, as amended at 64 FR 26287, May 14, 1999]

← § 640.102 Manufacture of Immune Globulin (Human).§ 640.104 Potency. →