Measures to minimize cross-contamination risks in Advanced Therapy Medicinal Product manufacturing

Current European regulations define in vitro expanded cells for clinical purposes as substantially manipulated and include them in the class of Advanced Therapy Medicinal Products to be manufactured in compliance with current Good Manufacturing Practice. These quality requirements are generally thou...

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Bibliographic Details
Main Authors: Livia Roseti, Marta Serra, Brunella Grigolo
Format: Article
Language:English
Published: ScienceOpen 2014-11-01
Series:ScienceOpen Research
Online Access:https://www.scienceopen.com/document?vid=0af59c6f-7bac-44a9-8164-ce0c06b5192b