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mondotwin/mondotwin-researcher

v0.7.4

Seven clinical-research skills on mondoTWIN's trial-registry and regulatory-guidance database: benchmark similar trials, count and compare registered trials with read-only SQL, report which endpoints and comparators the trials of an indication used and how they fared, review a protocol section against ICH, draft eligibility criteria from comparable trials, choose endpoints and estimands, and look up ICH or FDA guidance with quoted passages. Includes the mondoTWIN connector (OAuth sign-in).

guidance-lookup

Answer a question about ICH or FDA regulatory guidance with the exact passage quoted, the guideline id and the section. Use when the user asks what ICH (for example E6(R3), E8(R1), E9(R1), E10, M11, the Q series) or FDA guidance says about a topic, wants the source or exact wording of a regulatory expectation, or wants to check a statement against the guidance.

Read SKILL.md at the source

Pinned to revision 345a8357bd24, so it is the text this page describes rather than whatever the author pushed since.

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