Solutions
Scientific-to-Clinical Transition Messaging
Pipeline & Asset Storytelling
AutoBio bridges preclinical science and clinical development by translating mechanistic hypotheses into clinically relevant rationale. The platform connects biology, target validation, and early data into structured transition narratives.
Experts shape interpretation — deciding what carries forward, what must be reframed, and where claims should narrow as programs enter human studies. This ensures continuity without overstating early promise.
Typical Outputs
Preclinical-to-clinical transition narrative
Clinical rationale framing document
Claim narrowing and continuity guidance
Internal transition alignment materials
Transition risk and credibility assessment
Primary Users
Translational Medicine teams converting mechanistic rationale into clinical intent
Early clinical teams aligning study hypotheses and endpoints to scientific framing
Medical Affairs leaders preparing first-in-human narratives for scientific exchange
Governance committees evaluating readiness based on credibility and continuity of claims
Guardrails against hallucination and scientific drift
Structured workflows, evidence grounding, and expert oversight prevent unsupported claims, confabulation, and narrative overreach.
Claim-level citation and source traceability
Scientific and medical assertion is linked to underlying data, literature, or approved internal sources, with full transparency on inputs used.
Autonomous execution within defined scientific constraints
AutoBio executes multi-step workflows independently—within the boundaries of your data, instructions, and governance rules.
Proactive clarification to resolve ambiguity
The platform identifies gaps, conflicts, or unclear inputs and autonomously prompts follow-up questions before proceeding.
