Are Sterile Bioprocess Containers A Source Of Particulate Contamination?

Content Summary

We suggest that containers which are not produced to a recognized standard of cleanliness are a potential source of contamination.’ This article discusses why this is a problem for biopharmaceutical and vaccine manufacturers, the nature and source of possible contaminants, and a readily available solution.

Access this content

Choose an option below

Register to access this content

Your Work Email

Your Full Name

Your Company

Your Job Function

You might also be interested in

What to Know About Clean-in-Place (CIP) Systems

One much-favored equipment cleaning strategy throughout the food, beverage and dairy industries is the clean-in-place method.

A Comprehensive Approach for Solid Form Selection in Preclinical Development and Beyond.

Different solid forms (polymorphs, salts, cocrystals) of an active pharmaceutical ingredient (API) can have very different physico-chemical properties. Those differences can...

High-Throughput Sterile Filtration of Highly Viscous Pharmaceutical Formulations

In this work, high-pressure sterile filtration (HPSF) is presented as a method to increase yield without compromise on patient safety or product quality