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The success of Adeno Associate Vector (AAV)-based gene therapies rely on production platforms that can ensure high quality, large scale an..
In 2 weeks and 1 day
26 May 2021 at 17.00 CEST
On demand webinars
The number of ATMP therapeutic-based medicines for inherited genetic disorders is in constant growth, with a global 32% increase in new cl..
AAVs are the most promising viral vector for gene therapy thanks to their broad tropism and non-integrating properties. The current challe..
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