Enables AI agents to query free biomedical and pharmaceutical APIs for clinical trials, drug data, molecular structures, adverse events, and research literature.
Enables querying FDA medical device regulatory databases including 510(k) clearances, PMA approvals, recalls, and adverse events through natural language.
Enables AI assistants to query FDA drug labels, FAERS adverse event reports, recalls, and ClinicalTrials.gov trials, and to compute pharmacovigilance signal metrics such as PRR/ROR with confidence intervals and flags. It also provides a drug safety brief prompt that combines these sources with source links and limitations.