Webinar Date/Time: Tue, May 16, 2023 11:00 AM EDT
Non-infectious mock virus particles that mimic the physicochemical properties of live infectious viruses can be used as spiking agents during viral clearance testing. Review results from several studies using economical spiking surrogates – MVM and RVLP mock virus particles—to demonstrate viral clearance in industrial processes.
Register Free: https://www.biopharminternational.com/bp_w/viral-clearance
Event Overview:
To determine viral clearance efficacy of biomanufacturing steps, viruses are “spiked” into in-process solutions, processed and analyzed for reduction. Due to the infectivity of these viruses, studies are conducted in BSL-2 facilities. Costs and logistics limit analysis during process development. Discussed in the presentation are results from several studies that utilized non-infectious Mock Virus Particles (MVP’s) as MVM and RVLP surrogates. The results demonstrate the feasibility and value of adding viral clearance predication to downstream process development and optimization.
Key Learning Objectives:
Featured Speaker:
David Cetlin
Sr. Director, MockV Products
Cygnus Technologies
David Cetlin is the Senior Director of MockV Products at Cygnus Technologies, LLC. Mr. Cetlin founded MockV Solution in 2013 and was CEO until its acquisition by Cygnus in 2020. His lab is dedicated towards establishing a series of BSL-1 compatible viral clearance prediction kits. These kits aim to benefit downstream purification scientists as they develop, characterize, and validate their downstream purification processes.
Register Free: https://www.biopharminternational.com/bp_w/viral-clearance
Trump Directs FDA, EPA to Reduce Regulatory Barriers to Domestic Pharma Manufacturing
May 7th 2025The White House is instructing FDA to increase fees for and inspections of foreign drug manufacturing plants and reduce the time required to approve such sites that will be newly constructed in the US.
Trump Directs FDA, EPA to Reduce Regulatory Barriers to Domestic Pharma Manufacturing
May 7th 2025The White House is instructing FDA to increase fees for and inspections of foreign drug manufacturing plants and reduce the time required to approve such sites that will be newly constructed in the US.
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