← All industries
Accelerate clinical and regulatory work — without breaking GxP.
Document-heavy workflows from protocols to pharmacovigilance get faster, cleaner, and more auditable with AI agents that understand your data — and your regulators.
Book a Discovery Call →Why this industry is hard for AI
- !CFR 21 Part 11, GxP, and validation requirements make 'move fast' a liability.
- !Critical knowledge is buried across protocols, CSRs, SOPs, and safety reports.
- !Every AI output must be traceable, reproducible, and inspection-ready.
How we solve it
- ✓Validation-aware pipelines with versioning, audit trails, and reproducibility built in.
- ✓Retrieval grounded in your controlled documents — with citations on every answer.
- ✓GxP-aware review workflows so QA signs off before anything ships.
Top use cases for Life Sciences & Pharma
Regulatory Submission Drafting
Assemble and cross-check submission sections against source documents.
Pharmacovigilance Triage
Detect and prioritize adverse-event signals from case narratives.
Protocol & CSR Search
Ask questions across thousands of protocols and study reports.
SOP Compliance Checks
Flag deviations and missing steps against controlled procedures.
Compliance & Trust
CFR 21 Part 11GxPSOC 2ISO 27001
Validation documentation, audit trails, and reproducible runs for inspection readiness.
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Signal triage that took a week now takes an afternoon — fully traceable.
Head of Drug Safety · Global Pharma
Book an industry-specific Discovery Call
Tell us your Life Sciences & Pharma workflows — we'll map the highest-ROI AI opportunities for your team.
Book a Discovery Call →Have a Project? Talk to the Founders Directly
It's free, what do you have to lose?