businessHosted by U.S. Food and Drug Administration (FDA)
An FDA virtual town hall focused specifically on medical device biocompatibility and recent updates to ISO 10993-1:2025. FDA will discuss risk assessment approaches for biocompatibility endpoints, including material-mediated pyrogenicity and systemic endpoints.
Date
Time
01:00 PMPlatform
Online
Global
Hosted By
U.S. Food and Drug Administration (FDA)
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