Viral Clearance: The Basics On How To Conduct Effective Studies
Source: Cytiva

Several bioprocess steps contribute to viral clearance
To asses viral safety when validating a biomanufacturing process, you should study any step you claim to be reducing virus load. This assessment is usually done through a viral clearance study.
The results of the study are used as indirect evidence that the process can inactivate or remove viral contamination. Two types of biomanufacturing steps can provide viral reduction (Fig 1):
- Steps dedicated to virus inactivation or removal, such as pH treatment and heat treatment
- Steps contributing to viral clearance, such as chromatography steps dedicated to purifying the product, but with a potential to provide viral reduction
This article provides the basics of what you need to know when studying virus reduction of a chromatography step.
access the White Paper!
Log In
Get unlimited access to:
Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue.
X
Enter your credentials below to log in. Not yet a member of Outsourced Pharma? Subscribe today.
Subscribe to Outsourced Pharma
X
Subscribe to Outsourced Pharma
Cytiva
This website uses cookies to ensure you get the best experience on our website. Learn more