Literature DB >> 8174806

Considerations in performing virus spiking experiments and process validation studies.

A J Darling1.   

Abstract

Virus safety of blood and plasma products produced on an industrial scale depends on several procedures including the ability of the production process to remove or inactivate potential virus contaminants. Because of the highly variable nature of the starting material it is essential to measure the viral clearance capacity of the production process in order to give a high degree of assurance that a particular product will not be contaminated with infectious virus.

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Year:  1993        PMID: 8174806

Source DB:  PubMed          Journal:  Dev Biol Stand        ISSN: 0301-5149


  1 in total

1.  Specification-driven acceptance criteria for validation of biopharmaceutical processes.

Authors:  Lukas Marschall; Christopher Taylor; Thomas Zahel; Marco Kunzelmann; Alexander Wiedenmann; Beate Presser; Joey Studts; Christoph Herwig
Journal:  Front Bioeng Biotechnol       Date:  2022-09-23
  1 in total

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