Continual Learning in Medical Devices: FDA’s Action Plan and Beyond

Vokinger KN, Feuerriegel S, Kesselheim AS - Lancet Digital Health

  • Regulation and Clinical Evidence

Summary:

The authors discuss the regulatory challenges of AI/ML medical devices capable of continual learning, noting that no such adaptive device has yet been FDA-approved. Known risks, including dataset shift, bias, and catastrophic forgetting, require novel regulatory frameworks.

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International Regulatory Status and Reimbursement Recommendations of Haematological Malignancy Drugs Withdrawn from the FDA Accelerated Approval Pathway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