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Accelerated Clinical Trials

Accelerate the end-to-end clinical trial process

For clinical leaders at Sponsors and CROs, ACT automates workflows to shorten trial timelines and get to market quicker.

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Achieve faster, smarter, and cost-effective trials

Streamline trials with AI to save time, cut costs, and boost success rates.

Your priority
How we deliver impact
Accelerate trial timelines significantly
Cut trial time
ACT automates workflows, cutting trial timelines by 10-20 months, enabling faster delivery of therapies to market.
Reduce operational costs effectively
Minimize costly amendments
By leveraging AI-driven efficiencies, ACT minimizes costly amendments and streamlines processes, saving millions.
Enhance trial success rates reliably
Better trial outcomes
ACT uses predictive modeling to optimize study designs, site selection and improve enrollment for better trial outcomes.

Impact at scale

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Impact at scale

Clinical Trial Metrics

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Build smarter, cost-effective trials

AI-Driven Study Design

Streamline protocol creation with predictive modeling, reducing costly amendments and ensuring practical, goal-aligned designs.

Automated Site Selection

Prioritize high-performing sites using AI tools, cutting activation timelines and eliminating non-productive locations.

Real-Time Monitoring

Gain actionable insights with centralized workflows, addressing risks proactively to avoid delays and disruptions.

Integrated Data Systems

Unify real-world and proprietary data for seamless decision-making, enhancing trial efficiency and outcomes.

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Core capabilities driving impact

Identify real-world cohort scenarios

Translate protocol criteria into real-world patient cohorts using AI tools and curated data to assess feasibility and optimize patient selection early.

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Optimize study design

Optimize protocols with predictive AI, mitigate amendment risks, and save $1-6M per trial by aligning designs with real-world data and standards of care.

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Drive better site selection

Prioritize high-performing sites using AI-driven tools, reducing non-productive sites by 25% and site activation timelines by 1-2 months.

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Monitor trial health

Trial Health monitors sites, delivering real-time risks, next-best actions, and operational intelligence. ​
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Learn more about ACT

See how leading organizations use AI and real-world data to streamline study design, reduce delays, and bring therapies to patients faster

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ACT White Paper Render

See how leading organizations use AI and real-world data to streamline study design, reduce delays, and bring therapies to patients faster

Download ACT case study

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