Global cell and gene therapy lobby group The Alliance for Regenerative Medicine (ARM) has published a new report, highlighting key policy proposals to advance the sector.
The document brings together the views of a number of European policymakers, experts and drug developers, providing a comprehensive review of the regulatory and market access framework in Europe, and identifying potential hurdles to adoption.
The ARM argues that, while regulatory frameworks have been implemented to ensure approval of cell and gene therapies, payers and health technology assessment (HTA) bodies have not evolved mechanisms to implement the latest innovations, creating possible barriers post-approval.
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