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FDA now allows anonymized real-world data in medical device reviews to speed up approvals.
The FDA has updated its guidance to allow the use of de-identified real-world evidence in medical device applications, removing the need for identifiable patient data.
This change enables reviewers to use anonymized data from sources like cancer registries, insurance claims, and electronic health records, accelerating evaluations and expanding access to valuable insights.
The move aims to speed up patient access to life-changing therapies by unlocking vast, privacy-protected datasets.
The FDA may extend similar changes to drug and biologic applications in the future.
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La FDA ahora permite datos anonimizados del mundo real en revisiones de dispositivos médicos para acelerar las aprobaciones.