
Compare post-market surveillance for locked vs. continuous learning AI devices. Analyze regulatory guidelines, algorithmic drift, and validation strategies.

Compare post-market surveillance for locked vs. continuous learning AI devices. Analyze regulatory guidelines, algorithmic drift, and validation strategies.

Understand FDA SaMD classification for AI/ML devices. Review risk levels (Class I-III), 510(k) pathways, and regulatory guidelines for medical software.
Learn about the FDA's AI/ML medical device tracker. With 1,451 devices authorized through 2025 and 295 cleared in 2025 alone, we analyze authorization trends, specialty breakdown, foundation model milestones, and the evolving regulatory framework

Updated 2026 guide to FDA animal drug regulation: how CVM approves veterinary drugs, key differences from human drugs, recent approvals, antimicrobial stewardship, and telemedicine rules.
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