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FDA Addresses Medical Product Misinformation For The Post-COVID World

 
• By Hannah Daniel

The FDA’s updated guidance on internet responses to misinformation adds considerations for a post-COVID, social media influencer world. 

• Source: Shutterstock

With every new website or app, there springs a new avenue for misinformation, and 10 years after it first addressed the topic, the US Food and Drug Administration has updated its advice for device and drug makers looking to combat it.

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Guidance Feedback Highlights Outstanding Questions In AI Development

 
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Many of the hundred-plus commenters to the FDA's draft guidance on AI in medical product regulation said the document was a good start but needed additional clarity and more concrete examples. Stakeholders recommended the inclusion of case studies, metrics, and clearer guidelines to enhance the utility of the guidance, which is seen as a vital step for AI integration in healthcare.

IMDRF Offers Granular Playbook On ‘Regulatory Reliance’ Program Development And Implementation

 
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HIMSS 2025: Interview with Aneesh Chopra, Arcadia’s Chief Strategy Officer, About The Future Of Health Data, Interoperability, AI

 
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Global Medtech Guidance Tracker: March 2025

 
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AI-Based Screening Tool For Musculoskeletal Issues Gets US FDA Warning Letter

 
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New CLIA Rule Updates Personnel Policies

 
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