The effects of flux on the clearance of minute virus of mice during constant flux virus filtration

Author:

Fan Rong1,Namila Fnu1,Sansongko Davar2,Wickramasinghe S. Ranil2,Jin Mi3,Kanani Dharmesh3,Qian Xianghong1ORCID

Affiliation:

1. Department of Biomedical Engineering University of Arkansas Fayetteville Arkansas USA

2. Department of Chemical Engineering University of Arkansas Fayetteville Arkansas USA

3. Biologics CMC Teva Branded Pharmaceutical Products R&D, Inc West Chester Pennsylvania USA

Funder

Teva Pharmaceutical Industries

Publisher

Wiley

Subject

Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Reference25 articles.

1. Asher D. R. Katz A. B. Khan N. Z. &Mehta U.(2017).Methods of producing high titer high purity virus stocks and methods of use thereof. Google Patents.

2. Adapting virus filtration to enable intensified and continuous monoclonal antibody processing;Bohonak D. M.;Biotechnology Progress,2020

3. Normal-flow virus filtration: detection and assessment of the endpoint in bioprocessing

4. CPMP I.(1997).Q5A. Note for guidance on quality of biotechnological products: Viral safety evaluation of biotechnology products derived from cell lines of human or animal origin. (CPMP/ICH/295/95).http://www.emea.eu.int

5. Continuous viral filtration for the production of monoclonal antibodies

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