Transform complex protocols into clear, actionable tools
From informed consent to feasibility planning, Humantrue helps CROs get more done, faster.
Clinical trial protocols are complex, nuanced, and constantly evolving.
Clinical trial protocols are complex, nuanced, and constantly evolving. Our secure AI platform helps CROs streamline operations by acting as a dedicated, always-on protocol expert, reducing manual interpretation, minimizing inconsistencies, and improving trial efficiency from day one.
Move faster, but with certainty
Automating the generation of essential trial documents like informed consent forms and screeners saves significant time and reduces manual errors. Built-in quality assurance, powered by real-time data verification, expert oversight, and specialized models, ensures outputs are accurate, compliant, and reliable at every step.
Better decision making
Providing instant, smart answers to complex protocol questions empowers teams to make informed decisions quickly. This enhances operational efficiency, reduces protocol deviations, and supports faster, more accurate trial execution across sites.
Consistency and compliance
By centralizing protocol interpretation, you reduce the risk of misinterpretation and ensure regulatory compliance across documents. Managing multiple studies and collaborating with diverse stakeholders, this centralized approach streamlines communication, improves consistency in site training and documentation, and minimizes costly delays caused by protocol deviations or audit findings.
ROI for CROs
Deliverable:
Informed Consent Drafting
Current Process:
2-3 days
With HumanTrue:
10-30 minutes
Time Savings:
90%+
Cost Impact:
Equivalent cost, faster delivery
Deliverable:
Site Training Guide Development
Current Process:
3-5 days
With HumanTrue:
< 1 hour
Time Savings:
95%
Cost Impact:
Staff capacity preserved
Deliverable:
Patient Screener Development
Current Process:
2 days
With HumanTrue:
< 30 minutes
Time Savings:
85%
Cost Impact:
Faster recruitment start
Deliverable:
Clinicaltrials.gov Summary
Current Process:
1-2 days
With HumanTrue:
15-20 minutes
Time Savings:
90%
Cost Impact:
Improve registry quality