Biomedical Engineering Reference
In-Depth Information
Colder Products. 2010. Steam-Thru Connections—Product description. Available:
http://www.colder.com/Products/SteamThruConnections/tabid/740/
Default.aspx .
Cole, G. 1998. Pharmaceutical Production Facilities: Design and Applications.
Pharmaceutical Science Series. London: Taylor & Francis, Informa Health Care.
Cole Parmer. 2010. Silicon Tubing—Product description. Available: http://www.
coleparmer.com/Catalog/product_view.asp?sku=9610500 .
Colton, R. 2007. Recommendations for extractables and leachables testing—Part 1.
BioProcess Int . 11: 36-44.
Colton, R. 2007. The extractables and leachables subcommittee of the bio-process sys-
tems alliance. Recommendations for extractables and leachables testing, part 1:
Introduction, regulatory issues and risk assessment. BioProcess Int . 12: 36-44.
Colton, R. 2008. Recommendations for extractables and leachables testing—Part 2.
BioProcess Int . 1: 44-52.
Colton, R. 2008. The extractables and leachables subcommittee of the bio-process sys-
tems alliance. Recommendations for extractables and leachables testing, part 2:
Executing a program. BioProcess Int . 1: 44-52.
Committee for Proprietary Medicinal Products (CPMP). 1996. Mark for guidance on
virus validation studies: The design, contribution and interpretation of studies
validating the inactivation and removal of viruses. CPMP/BWP/268/95.
Committee for Proprietary Medicinal Products (CPMP). 2000. Annex to Note for
Guidance on Development Pharmaceutics: Decision Trees for the Selection of
Sterilisation Methods. London: European Medicines Evaluation Agency.
Computational-fluid-dynamics (CFD) analysis of mixing and gas-liquid mass trans-
fer in shake flasks. Biotechnol. Appl. Biochem . 41: 1-8.
CPMP. 1996. Note for guidance on virus validation studies. The design, continuation
and interpretation of studies validating the inactivation and removal of viruses.
CPMP/BWP/268/95.
CPMP. 1997. Mark for guidance on quality of biotechnology products, viral safety
evaluation of biotechnology products derived from cell lines of humanly or ani-
mal origin. CPMP/I/295/9S. London.
CPT Consolidated Polymer Technologie, Inc. 2002. Material Comparison. Brochure.
Available: http://www.stilow.com/CFIex-Tubing-Material-Comparison.pdf .
Croughan, G. 2010. Beyond Just High Titers: The Future of Cell Line Engineering. IBC
Cell Line Development and Engineering Conference, San Francisco, CA.
Curling, J. and Gottschal, U. 2007. Process chromatography: Five decades of innova-
tion. BioPharm. Int . 21: 70-94.
Curtis, S., Lee, K., Blank, G.S., Brorsen, K., and Xu, Y. 2003. Generic/matrix evaluation
of SV40 clearance by anion exchange chromatography in flow-through mode.
Biotechnol. Bioeng . 84: 179-186.
Curtis, W.R. 1999. Achieving economic feasibility for moderate-value food and fla-
vour additives. In Fu, T., Singh, G., and Curtis, W.R. (eds.), Plant Cell and Tissue
Culture for the Production of Food Ingredients . New York: Kluwer Academic,
225-236.
Curtis, W.R. 2004. Growing cells in a reservoir formed of a flexible sterile plastic liner.
United States Patent 6709862B2.
D'Aquino, R. 2006. Bioprocessing systems go disposable. Chem. Eng. Prog . 102 (5):
8-11.
Search WWH ::




Custom Search