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AKRA TEAM provides regulatory affairs consultancy for medical devices, in-vitro diagnostics, and combination products. They support clients with compliance to EU MDR and IVDR regulations, quality management systems, technical documentation, clinical evaluations, and post-market surveillance. The company has a strong reputation for expertise in navigating complex healthcare regulations and ensuring timely market access for safe medical technologies[1][2][3].
They do not have their own clinical pipeline or results as they are a service provider.
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