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Virus Safety
Virus Safety - Your Process. Our Expertise. A committed partnership.

Regulatory guidance advocates virus control at various stages of the drug manufacturing process, directing that you:

  • Select and test source materials for the absence of virus
  • Test the capacity of the production process to remove or inactivate virus
  • Test the product at appropriate stages of production for detectable virus

Partnering with a company that can assist you through all of these critical steps is an important factor. Explore our areas below, including our Virus Filtration products, to see how we can help ensure viral safety.

New to Virus Safety or looking for best practices?
Visit our Virus Safety Learning Center
View our Webinars

Viresolve® Pro+ Solution Magnus Holder Interactive Guide - Learn More
Process development Towards a robust and economically-sized virus filtration process - Webinar
Virus Safety Resources
Technical Literature
Events
Services
Meet Your Virus Safety Team
Featured Team Member
Ashley Slocum
Ashley Slocum, Biomanufacturing Engineer
Claim to Fame: Thought leader in virus prep purity
Specialy Area: Virus filtration
Education: Northeastern University, BS Chemical Engineering
Fun Fact: I am an identical twin.
Publications:
  • Slocum, A., Burnham, M., Genest, P., Venkiteshwaran, A., Chen, D., Hughes, J. 2012. "Impact of Virus Preparation Quality on Parvovirus Filter Performance". Accepted for 2012 publication in Journal Biotechnology and Bioengineering.
  • Asher, D., Slocum, A., Bergmann K., Genest, P., Katz, A., Morais, J., Lawrence, C., Greenhalgh, P. 2011. "Predicting Virus Filtration Performance with Virus Spike Characterization", BioProcess International, 9(3): 26-27.
Raw Materials Chromatography Virus Filtration
Raw Materials
Chromatography
Virus Filtration