Summary:Describes a method for determining the titer of viable (infectious) Pseudorabies Virus (PRV) through the enumeration of plaques formed in a monolayer of sensitive target cells. Intended for use in routine testing of cell lines, cell line derived products and for the support of process validations of systems that claim to remove or inactivate PRV. Describes a method for establishing and maintaining a PRV stock.Included Sections:Purpose, Scope, Responsibility, References and Applicable Documents, Materials and Equipment, Health and Safety Considerations, Documentation Requirements, and ProceduresIncluded Attachments/Appendices:NoneAbout This Document:This is not a generic template, it's a 7-page procedure that was actually created and used in the Bioprocessing operations of a FDA-regulated establishment. The company-specific information (names, addresses, some images, proprietary product information, etc.) has been redacted but the content and format have been largely preserved. Reasons to Buy:Use it as a starting point for your own documentation projectCompare the quality of your documents against your industry peersLearn what other companies in your industry are actually doingWho Will Benefit:Biologic Manufacturing PersonnelProcess Development PersonnelMethod Development Personnel