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FDA Refines Accelerated Approval Pathway with New Draft Guidance

XTalks

The US Food and Drug Administration (FDA) has released a new draft guidance titled Expedited Program for Serious Conditions Accelerated Approval of Drugs and Biologics Guidance for Industry refining the accelerated approval pathway for drugs and biologics targeting serious or life-threatening conditions.

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How FDA’s AI Draft Guidance Aims to Bring Transparency to Drug Development

XTalks

Transparency is especially important in addressing the ‘black-box’ nature , where users and regulators may not know why an AI model reaches a particular conclusion, which often makes these systems harder to trust. To comply, sponsors need to ensure AI models are transparent, reproducible and suited to their specific context.

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What the FDA’s Draft Guidance for AI-Enabled Medical Devices Means

XTalks

The FDAs new draft guidance for developers of AI-enabled medical devices marks a critical milestone in addressing the complexities of transparency, bias and safety throughout the lifecycle of these advanced technologies.