Meet Ash.
AI workflows for the way clinical teams actually work.

Ash connects study configuration, continuous data review, and clinical insights in a governed, auditable workflow model. Your qualified team retain accountability at every step.

Ready to Revolutionize Your Clinical Oversight?

See how Ash can de-risk your portfolio and accelerate your timelines.

Schedule a live, personalized demo with a platform specialist to see how Ash can address your specific trial challenges.

An ecosystem of workflows. One governance model. One clinical lifecycle.

Ash is a clinical AI agent embedded in the operational fabric of your trial — from the first study build through database lock and portfolio oversight.

Impact metrics

Early results from clinical teams using Ash

Real performance improvements from clinical teams using Ash. Our AI-powered clinical trial agent delivers measurable results across data review, compliance, and operational efficiency.

Secured for the enterprise with industry-leading compliance
SOC 2 | ISO 27001 | 21 CFR Part 11 | ICH E6 (R3)

370+ Hours saved per study per person through automation

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faster DRP config vs. traditional SAS-based methods
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data review program checks configured in ~5 weeks

Reviews data as fast as 4 full-time employees

Cost savings of $68.67 per hour through improved efficiency

Average time from setup to full deployment in 4 weeks

Average of 3 eligibility violations prevented per study

ASH FOR STUDY CONFIGURATION

From protocol upload to complete study draft — in days, not months

Study configuration has historically moved through spreadsheets and email, with every interpretation introducing variation before data collection begins. Ash changes the starting point.

  • Upload a protocol. Ash drafts the study tree, visits, forms, fields codelists, and edit checks — structured and ready for review.

  • Your team reviews the draft, provides comments, and releases. Ash handles the structured drafting work; your team retains full authority over what ships.

  • Configuration that has historically required months of specification cycles can now be completed in hours.

ASH FOR DATA MANAGEMENT

Continuous data review — surface issues before the next scheduled review

Listings, vendor files, and query trackers spread across disconnected systems scheduled review cycles surface issues weeks after data entry. Ash runs checks continuously against live study data.

  • Ash ingests data from EDC, eCOA, IRT, central labs, and CRO outputs without extensive IT involvement, working alongside your existing tech stack.

  • Clean Patient Tracker delivers per-subject readiness status, open blockers, and query history in a single view — no assembly required.

  • Every check produces a logged audit trail entry. Reviewers see the source evidence, make the call, and own the outcome.

ASH FOR INSIGHTS

Risk visible throughout the study — not discovered at lock

Problems surfaced only at the database lock are the most expensive to remediate. Ash for Insights brings lock readiness into continuous view, while a shared governance model protects every output across all Ash workflows.

  • Leverage our team’s extensive pharmaceutical experience to align oversight strategies with critical-to-quality (CtQ) factors.

  • Ensure compliance with ICH E6(R3) by focusing on protocol-specific risks and outcomes.

  • Prioritize data review efforts to enhance trial quality and regulatory readiness.

Customer Success Stories

Clinical teams use SiteroAI in research labs, remote offices, and wherever trials need oversight.

“Using SiteroAI saves me about 1.5 hours each day because everything I need is right there”

— Aurion Biotech Clinical Team

eCompliance Technology - Sitero

1.5 Hours Daily time saved per team person

66% Data review time reduction