Observed arrival · 2026-09-10
Indago: Regulatory AI With a Paper Trail
Indago turns a company’s regulatory documents into traceable drafts for FDA program work.
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The homepage illustrates a document-grounded workflow using a CTD 2.6.6 nonclinical example. Drafted prose about a 13-week rat study is broken into evidence items, including a 100 mg/kg/day NOAEL, reversible findings after a four-week recovery period, and an approximately 10-fold exposure margin. Each item carries an assertion identifier and points to a named PDF, page, and paragraph, making the proposed review trail visible rather than leaving provenance as a general promise.
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