Adapting viral safety assurance strategies to continuous processing of biological products

Author:

Johnson Sarah A.1,Brown Matthew R.1,Lute Scott C.1,Brorson Kurt A.1

Affiliation:

1. DBRRII, Office of Biotechnology Products, Office of Pharmaceutical Quality; Center for Drug Evaluation and Research, Food and Drug Administration; Silver Spring Maryland 20993

Funder

FDA/CDER's Research Review Coordinating Committee

Publisher

Wiley

Subject

Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Reference97 articles.

1. Chiral separations are enduring items in the toolbox;Anon;Chem Eng News Archive,2003

2. Clearance of the rodent retrovirus, XMuLV, by protein A chromatography;Bach;Biotechnol Bioeng,2015

3. Evaluation of viral inactivation efficacy of a continuous flow ultraviolet-C Reactor(UVivatec);Bae;Korean J Microbiol Biotechnol,2009

4. Design and synthesis of novel glycopolythiophene assemblies for colometric detections of Influenza Virus and E. Coli;Baek;Bioconjugate Chem,2000

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