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Managing Extractables & Leachables: Early Planning with Your CDMO

Published on Cell & Gene


Extractables and leachables (E&L) testing is a critical regulatory expectation in cell and gene therapy manufacturing. This article explains why engaging your CDMO early on E&L strategies can prevent delays, ensure regulatory alignment, and support product safety from the start.


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Images used are for illustrative purposes only and do not depict actual persons, products, or facilities. For full details, please refer to the original article via the provided link.

 
 
 

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