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As seen in: Pharmaceutical Online, Cell & Gene
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Articles

EMA Adopts Collaborative Approach With ATMP Guideline Update

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By Pam Dhadda, CMC Cell
| Pharmaceutical Online Verified
By Pam Dhadda, Associate Director, CMC Cell and Gene Therapy at PharmaLex The European Medicines Agency (EMA) has taken a significant step forward in the regulation of advanced therapy medicinal products (ATMPs) by releasing an updated draft guideline on the quality, non-clinical, and clinical requirements for these innovative therapies in clinical trials.
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