Query openFDA API for drugs, devices, adverse events, recalls, regulatory submissions (510k, PMA), substance identification (UNII), for FDA regulatory data analysis and safety research.
8.3
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Backend Development
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Excellent skill for FDA regulatory data access. The description clearly conveys queryable endpoints (drugs, devices, adverse events, recalls, 510k/PMA, UNII), enabling easy invocation. SKILL.md provides comprehensive task knowledge with detailed query patterns, examples, error handling, and pagination strategies. Structure is outstanding: concise main overview with well-organized sections and explicit references to detailed documentation files. The skill offers meaningful value by abstracting complex FDA API interactions, rate limiting, caching, and providing domain-specific query patterns that would otherwise require extensive documentation review and trial-and-error. Slight novelty deduction as API wrappers are common, but the comprehensive coverage of multiple FDA endpoints, pharmacovigilance patterns, and cross-database lookup strategies add substantial complexity reduction for CLI agents tackling regulatory research tasks.
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