European Medicines Agency. EMA’S GUIDE ON ADVANCED THERAPY MEDICINAL PRODUCTS. Non-Clinical Development Checklist. Version 1.0 – 29 November 2021

Published by EMA

Gene Therapy Medical Products Non-Clinical Development Checklist

EMA’s guide to help developers of gene therapy medicinal products (GTMPs) and cell-based medicinal products (CBMPs) navigate the most important regulatory requirements during the non-clinical development phase

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European Medicines Agency. EMA’S GUIDE ON ADVANCED THERAPY MEDICINAL PRODUCTS. Non-Clinical Development Checklist. Version 1.0 – 29 November 2021

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