Enables querying FDA regulatory metadata for drugs, biologics, and medical devices through the openFDA API, including resolving application numbers and product names to authoritative regulatory details.
Enables automated assessment of research manuscripts against the TARGET reporting guideline for target trial emulation, providing item-by-item scoring with evidence and provenance.
An MCP server implementing the ROBINS-I V2 framework for risk-of-bias assessment in non-randomized studies, with deterministic algorithms and full provenance. It enables users to parse study documents, specify target trial results, answer signalling questions with evidence-bound quotes, and compute or override domain judgements.