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Update on new guidance by the EMA  - Advanced Therapy Medicinal Products
Update on new guidance by the EMA - Advanced Therapy Medicinal Products
22/08/2019 17:34:41

The European Medicines Agency (EMA) yesterday released a questions and answers (Q&A) document specifically in relation to Advanced Therapy Medicinal Products (ATMPs), clarifying the circumstances in which an exemption from the normal requirement to re-test batches of medicinal products imported from third countries into the EU may be granted. 

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