Shuren At FDLI: Least-Burdensome, Real-World Evidence Efforts Picking Up

US FDA's device-center head discussed his continued push to make regulations more flexible, plans for least-burdensome training and what's next for NEST, among other topics, at the Food & Drug Law Institute annual gathering in Washington DC.

US FDA’s relatively slow path to market may cost small manufacturers more than $40m more than they’d spend in countries with easier device approvals, device-center head Jeffrey Shuren acknowledged at the Food & Drug Law Institute’s Annual Conference May 4 in Washington, DC.

The figure, which was compiled by Versant Ventures, includes $1.8m for eight extra weeks waiting to meet with FDA; $5.5m...

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MI-PolicyAndRegulation (Free-1): Biliary Atresia Linked to Autism and Neurodevelopment Delays

 
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Children with biliary atresia (BA) exhibited neurodevelopmental deficits and increased autism traits, with earlier surgery linked to better general neurodevelopment.

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News We’re Watching: New FDA Approvals For Breast Implant, Colon Cancer Test, Imaging Agent; TAP Expansion, AI Standards

This week, Establishment Labs Holdings announced the FDA gave it premarket approval for Motiva breast implant, Cologuard lands FDA approval for Cologuard Plus and GE HealthCare gets FDA nod for a new imaging agent. The FDA announces another expansion for TAP into ophthalmology and radiology. The AAMI and CTA will join forces to develop standards for AI and ML-enabled health care products.  

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Nancy Tests SPARC-931 Part 7

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