The Intelligent Agent for Risk-Based Oversight
Ash OSAre you ready to empower your team?
Ash Clinical Trial Agent™
Your Complete Toolkit for AI-Powered Study Oversight
Discover how Ash transforms every aspect of clinical trial management with intelligent automation
From biotech startups to Big Pharma
Clinical teams use studyOS in research labs, remote offices, and wherever trials need oversight.
Using studyOS saves me about 1.5 hours each day because everything I need is right there
Results with Ash
Hours saved per study per person through automation
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
Automate and Harmonize Review Workflows With Purpose-Built AI
Ash's embedded capabilities transform manual oversight into automated intelligence, integrating directly with your existing clinical systems under your brand.
- Utilize Ash, our Clinical Trial Agent™, to transform ad-hoc queries into consistent, automated workflows.
- Ash learns from each interaction, continuously improving its ability to flag critical issues and reduce noise.
- Establish sustainable oversight processes that adapt to evolving trial demands.
Seamlessly integrate with pre-existing investments
Traditional monitoring reports can't cover every compliance scenario. With Ash, compliance teams get instant answers to regulatory questions with complete audit trails.
- Seamlessly ingest data from EDC, eCOA, IRT, labs, and CRO outputs without extensive IT involvement.
- Achieve centralized visibility into trial data, facilitating informed decision-making.
- Overlay studyOS onto existing technology stacks, eliminating the need for disruptive system overhauls.
Understand Clinical & Regulatory Priorities
Clinical operations and data managers use Ash to test protocol adherence, validate site performance, and uncover study patterns instantly.
- 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.
Ready to Revolutionize Your Clinical Oversight?
See how Ash can de-risk your portfolio and accelerate your timelines.
See Ash in Action
Schedule a live, personalized demo with a platform specialist to see how Ash can address your specific trial challenges.
Request a Personalized Demo