Post by Alira Health

Why do some medical devices achieve regulatory approval but fail to gain adoption, reimbursement, or commercial success? In this interview from MedTech World North America, Mercè Guerra Albà, Associate Director of Regulatory Affairs at Alira Health, explains why regulatory approval alone is no longer enough for medtech companies and how a more integrated development strategy can improve market access and commercial outcomes. Planning to launch a medical device in the US or Europe? Explore how aligning regulatory requirements, evidence generation, market access, and patient needs early can help reduce delays and support successful market entry: https://lnkd.in/dR32Vkba

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