Challenges Faced by End Users During The Qualification of SUS
Posted on November 22, 2018
Ben Jeyaretnam, E&L Analytics Lead
Sanofi, Swiftwater, PA, USA.
All Single Use Systems (SUS) or components used during the manufacturing process must be qualified to prove that no compounds of safety concern will leach into the product stream or present in the final product, potentially compromising the integrity, purity, and efficacy of the medical products adm...
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Related Topics and Keywords
E&L qualification, leachable stability study, Qualification of SUS, Single-use Systems
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