NexTrial.ai is the AI orchestration layer for clinical trials. Collapsing site activation from 60–120 days down to 30–45 days with deterministic, regulatory-grade automation.

The challenge isn't speed. It's clarity.
Sponsors need confident FPI forecasts. CRO teams need consistent feasibility signals. Sites need relief from rework, queries, and protocol ambiguity.
We built the orchestration engine that brings clarity to all three.

What NexTrial Actually Does

We verify site capabilities, model patient trajectories, and activate naïve and experienced sites with regulator-grade confidence before the first Sponsor conversation.

• Feasibility, standardized and accelerated:
Clean capability signals. Operational, quality, staffing, documentation. Giving CROs and Sponsors clarity instead of assumptions.

• Predictive Eligibility (PPEE):
Most engines match criteria and hope the patient stays eligible. We model trajectory, tolerability, physiological stability, and behavioral dynamics to predict not only who might qualify, but who can tolerate the journey.

• Activation Intelligence (TAI):
Protocol ingestion → readiness scoring → document orchestration → zero-rejection IRB packets with full explainability.

• Regulatory-as-a-Service (RaaS):
FDA (US), CDSCO/ICMR (India), ANVISA/CEP (Brazil).
Regulatory alignment, preventable errors, and compliance logic are embedded and fully explainable.

This isn’t digitization.
This is clinical-grade orchestration, deterministic, auditable, and built for trust.

Who We Serve

• Pharma & Biotech teams needing predictable FPI forecasting
• CROs needing standardized feasibility and clean activation packets
• Hospitals & research centers overwhelmed by IRB cycles and rework
• PIs & naïve physicians entering research with guided, protocol-aware workflows

Why It Matters

When readiness is predictable, activation becomes a competitive advantage.
Documentation stays clean.
Eligibility becomes forecastable.
Execution aligns with plan.

NexTrial AI

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NexTrial AI

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