Query openFDA API for drugs, devices, adverse events, recalls, regulatory submissions (510k, PMA), substance identification (UNII), for FDA regulatory data analysis and safety research.
Conduct comprehensive, systematic literature reviews using multiple academic databases (PubMed, arXiv, bioRxiv, Semantic Scholar, etc.). This skill should be used when conducting systematic literature reviews, meta-analyses, research synthesis, or comprehensive literature searches across biomedical, scientific, and…
Follow-up questions ("what's the market cap?", "what do analysts say?") should use data from earlier tool responses before making new calls. If you already fetched a company profile or financials, surface that data directly.
Local readability checker for substantial English prose such as docs, PR descriptions, commit bodies, blog posts, and explanations. Measures Flesch Reading Ease (0-100, higher is easier), MTLD, and TTR. Use when the user asks to check, simplify, or rewrite prose. Aim for 60 unless the user specifies a different…
All tools that accept meeting identifiers use meetingid (not docid, id, or documentid). The meetingid value comes from the id field in search results and meeting lists.