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flag FDA now allows anonymized real-world data in medical device reviews to speed up approvals.

flag 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. flag 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. flag The move aims to speed up patient access to life-changing therapies by unlocking vast, privacy-protected datasets. flag The FDA may extend similar changes to drug and biologic applications in the future.

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