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COVID-19 Update Analytics Development Downstream Processing Manufacturing Outsourcing Quality/GMPs Upstream Processing 2020 Bio/Pharma Virtual Congress

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COVID-19 Update
Analytics
Development
Downstream Processing
Manufacturing
Outsourcing
Quality/GMPs
Upstream Processing
2020 Bio/Pharma Virtual Congress

TopicSee All >

Analytical Methods
BioBusiness
Cell Culture/Fermentation
Continuous Processing
Drug Delivery
Fill/Finish
Formulation
Process Chromatography
Process Control/PAT
Process Development
QA/QC
Separation and Purification
Single-Use Systems
Supply Chain

About Us
Advertise
Editorial Information
Contact Us
Do Not Sell My Personal Information
Privacy Policy
Terms and Conditions

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Predicting Viral Clearance at Your Benchtop

July 27, 2020

Biopharma Insights - Thought Leadership from Marketers | Paid Program

Viral contamination is an inherent risk during the manufacture of therapeutic products such as antibodies, vaccines, viral vectors, and plasma derivates.