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26 June 2020 | By Brendan Tindall (bioMerieux), Kevin Williams (bioMerieux)
For over 30 years, pharmaceutical and medical device product release has relied solely on endotoxin assays using Limulus Amebocyte Lysate (LAL). This article addresses the potential risks associated with relying on a single raw material in a fragile supply chain and explores alternative testing options.
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