Medcon 2023: Shuren Mulls New Pathway For Digital Devices

The head of the US FDA’s Center for Devices and Radiological Health said that an optional new pathway could help the agency regulate the flood of novel devices intended for at-home use. His presentation also touched on MDUFA V implementation, post-pandemic strategy, and CDRH staffing needs.

alternate pathways
• Source: Alamy

The US Food and Drug Administration may need to create a better pathway for the regulation of software-based devices, device center head Jeff Shuren said on 25 April at Medcon 2023 in Columbus, OH.

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US FDA Teleconferences In As IMDRF Gathers In Tokyo

 
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The International Medical Device Regulators Forum discussed AI regulation, the development of a reliance playbook, and post-market regulation at the group's annual meeting in Tokyo last week. While the US FDA was not on-site, the agency was able to participate virtually.