[synthesis.]Internal

Regulatory intelligence — not medical or legal advice.

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Runs once per app session in the background and keeps existing data if source APIs are unavailable.

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Ask · OpenAI

Requires OPENAI_API_KEY on the server. Heuristics always run first.

Diligence — limitations & disclaimer

Who this is for

Asset × indication diligence for people in biotech — funds, biotech and pharma teams, and sophisticated self-directed researchers. Not mass-market retail investing.

What it is

A structured, evidence-linked memo built from a persisted public regulatory and trials graph (FDA label-quality links, outcomes, analogs) with optional live supplements (ClinicalTrials.gov, PubMed) clearly labeled T3.

What it is not

  • Not investment advice, buy/sell, or partner recommendations
  • No numeric probability of success or valuation
  • Not a substitute for primary sources, dataroom review, or licensed commercial data
  • Private or proprietary documents are not ingested in the public pilot (M3+)

Coverage honesty

Reports disclose graph coverage (trials, targets, label-quality links). Thin coverage triggers live supplements; gaps remain explicit in the evidence-quality domain.

Evidence tiers

  • T1 — persisted public graph
  • T3 live — fetched at run time, not yet ingested
  • T3 project — user-provided assumptions/documents (when enabled)

See handoff/DILIGENCE_PRODUCT_ROADMAP.md for milestone scope. Questions: contact the synthesis operator.

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