Enables AI agents to query and analyze FDA adverse events, drug labels, medical device clearances, and other public health datasets through natural language commands.
Provides LLM-optimized access to FDA data through the OpenFDA API and direct regulatory decision document retrieval, covering all 21 OpenFDA endpoints plus 510(k) summaries, De Novo decisions, and PMA approvals.
Enables AI assistants to retrieve, search, and track changes to US Code of Federal Regulations sections via the eCFR API, returning actual regulation text with citations and point-in-time date support.
Enables querying FDA medical device regulatory databases including 510(k) clearances, PMA approvals, recalls, and adverse events through natural language.