Sterile Filtration and Virus Filtration

Author:

Kuriyel Ralf,Zydney Andrew L.

Publisher

Humana Press

Reference7 articles.

1. Food and Drug Administration (1987) Guideline on sterile drug products produced by aseptic processes. Center for Drugs and Biologics, Office of Regulatory Affairs, Food and Drug Administration, Rockville, MD.

2. Emory, S. (1989) Principles of integrity testing hydrophilic microporous membranes. Pharm. Technol. 13, 68–77.

3. PDA Sterile Filtration Committee (1977) PDA Technical Report No. 26: Sterilizing filtration of liquids, Parenteral Drug Association, Bethesda, MD.

4. Ho, W. S. W. and Sirkar K. K. (1992) Membrane Handbook, Van Nostrand Reinhold, New York.

5. DiLeo, A. J., Vacante, D. A., and Dean, E. F. (1993) Size exclusion removal of model mammalian viruses using a unique membrane system, Part I: membrane qualification. Biologicals 21, 275–286.

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