Schedule demo
See 6 months of work done in days Schedule demo

Quinn, the AI Scientist.
6 months of analysis. Done in days.

Drug discovery to commercialization. You bring the data and objective. Quinn brings decision-ready results. Fully traceable. Your IP, always.

Schedule demo Learn more
Your IP, 100% · Never trains on your data · SOC 2 Type II
Trusted by teams at

How Quinn works

Scope

Data + Objective. That's it. Messy CSVs, PDFs, legacy formats. Quinn handles the cleanup.

Technical details
  • Read-only connectors for ELN/LIMS, S3/GCS/Azure, Snowflake, Databricks
  • Automatic lineage tracking and metadata capture (FAIR-compliant)
  • No data movement required - your data stays where it is
  • Ingests raw, unstructured data and harmonizes automatically

Analyze

50-100 iterations. Like a team of scientists in a lab meeting, challenging every conclusion.

Technical details
  • Established methods your teams already use, executed automatically
  • Internal critique loops that poke holes and refine approach
  • Science, regulatory, and commercial analysis run in parallel
  • Environment pinning for perfect reproducibility
  • Auto-scaling across HPC, Kubernetes, AWS/Azure/GCP

Deliver

Decision-ready results. Validation blueprints. Every claim traceable and auditable.

Technical details
  • Go/no-go recommendations with explicit rationale
  • Validation blueprints: what to do next, why it matters, what success looks like
  • Every claim auditable. Your team can verify any step
  • Protocol-ready experimental designs for lab confirmation
  • Electronic signatures and audit-ready trails
  • Full citations and references for regulatory submission

Proven acceleration

3 months → 4 days
Target discovery
5 novel targets with go/no-go rationale
4 months → 4 days
Trial design
10K simulations → FDA-aligned protocol
Never → 3 days
Competitor failure analysis
Why they failed. What you need to change.

From discovery through commercialization

1
Discovery
Target ID
MoA elucidation
Biologics design
2
Pre-Clinical
Lead optimization
Animal models
CMC & synthesis
3
Clinical
Trial design
Site selection
Biomarker ID
4
Regulatory
IND gap analysis
Safety summaries
Submission prep
5
Strategy
TPP & valuation
Competitive intel
Asset repurposing

Built for your teams

Discovery & Comp Bio
Target ID to lead selection in days
CMC & Process
Synthesis routes, specs, regulatory-ready
Clinical Operations
Trial design, site selection, biomarkers
Regulatory & Strategy
IND prep, safety summaries, valuations
Our team quoted 6 months for the competitive analysis. Quinn finished it over the weekend.
VP Strategy, Global Pharma

Your IP. Your data. Always.

100% IP ownership Never trains on your data SOC 2 Type II ISO 27001 HIPAA Your cloud or ours

Built by Stanford computational scientists who've spent decades in pharma R&D Backed by Y Combinator

See 6 months of work done in days

30-minute walkthrough. Bring a real question. We'll show you what Quinn delivers.

Schedule your demo