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.