Your Team.
Your Timeline.
No More Trial Delays.
The first AI agent purpose-built for clinical trial workflows. Take control of SDTM creation, CRF generation, any workflow you need—executed on your schedule, to your standards, without dependency delays.
Urgent: We need SDTM datasets for the Phase III cardio study by Friday for the FDA submission. The contractor is saying it'll take 3 weeks minimum. We're completely blocked! 😰
@baseline can you help us out here?
✅ I'll handle the SDTM creation for your Phase III cardio study. Processing your data now - expect a reviewable draft conversion in 1hr with full CDISC compliance and validation reports.
Every Study Faces the Same Delays.
Until Now.
Your teams know the pattern: vendor promises slip, data packages arrive late, submissions get pushed. The real question is what it's costing you.
Today: $302K Lost Per Phase III Day
Every delayed day costs $302,200 in lost revenue plus operating expenses. That's real money, not theoretical.
$10M+ saved in accelerated timelines
Today: Weeks Lost in Vendor Back & Forth
Endless email chains, revision cycles, scope clarifications, and approval processes. Simple requests become multi-week negotiations.
Clear instructions, immediate results, no negotiations
Today: $56K Daily Phase III Operations
Plus $24K in Phase II, $8K in Phase I. Operating costs pile up during vendor delays and bottlenecks.
Eliminate waiting time and blockers
Three Ways to Transform.
One Powerful Platform.
Pre-made workflows for instant productivity. AI agent collaboration through RStudio. Custom workflow development for unique needs. Baseline adapts to how your team works.
Pre-Made Workflows
Ready-to-use SDTM creation, CRF generation, and data validation workflows. Deploy immediately without setup.
AI Agent Collaboration
Work directly with our AI agent in RStudio. Natural language requests, real-time collaboration, your data never leaves your environment.
Custom Development
Need something unique? Our team builds custom workflows tailored to your exact requirements and validates them on your data.
Built for Clinical Research Compliance
Your data security isn't an afterthought—it's the foundation of everything we build.
HIPAA Compliant
Full compliance with healthcare data protection requirements and privacy standards.
CFR 21 Part 11 Compliant
Electronic records and signatures compliance for pharmaceutical and clinical research.
Full Data Transparency
Complete visibility into data processing with comprehensive logging and audit capabilities.
Imagine your organization
12 months from now
Partner with us to build
the future of clinical research
Ready to transform how your organization runs clinical trials? Let's discuss how our platform can accelerate your research timeline and improve data quality.
