The Watchman Saga—Closure at Last?

Kramer DB, Kesselheim AS - New England Journal of Medicine

  • Regulation and Clinical Evidence

Summary:

The authors trace the regulatory history of the Watchman left atrial appendage closure device, which was available in Europe for nearly a decade before US approval, highlighting differences between US and EU device regulation and the importance of requiring clinical evidence for high-risk implantable devices.

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Recent Work from PORTAL

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How Congress Can Fix Expert Advisory Committees

Daval CJR, Kesselheim AS - STAT

  • Regulation and Clinical Evidence
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International Regulatory Status and Reimbursement Recommendations of Haematological Malignancy Drugs Withdrawn from the FDA Accelerated Approval Pathway

Mulsant SS, Kesselheim AS, Naci H - Journal of Cancer Policy

  • Price, Value, and Access
  • Regulation and Clinical Evidence
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Comments on FDA Discussion Paper, “Considerations for the Regulation of Generative AI-Enabled Medical Devices”

Jaiswal N, Gorijavolu R, Thomas S, Hwang TJ, Celi LA, Kesselheim AS - Food and Drug Administration (FDA)

  • Regulation and Clinical Evidence