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FDA approves
new sterile filling facility for Bayer Biological Products
News Release Apr., 30/RESEARCH TRIANGLE PARK, N.C., / -- Bayer Biological
Products (BP) announced it received approval from the Food and Drug Administration
(FDA) for its new sterile filling facility (SFF) at the company's Clayton,
North Carolina, manufacturing plant. The FDA approval marks a significant
milestone for Bayer BP and the Clayton facility, where Bayer BP manufactures
life-saving, plasma-based therapeutic proteins.
The SFF will be used for final container filling, freeze-drying, and
pasteurization of all products manufactured in Clayton including Prolastin,
Alpha1-Proteinase Inhibitor (Human), used in the treatment of genetic
emphysema, Gamimune N, Immune Globulin Intravenous (Human), indicated
for patients with immune deficiencies, and Koate-DVI Antihemophilic
Factor (Human), used to treat hemophilia.
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Source: Information about Bayer Biological Products Division can be found at www.bayerbiologicals.com.
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