We understand clinical trials like you do
Smarter starts. partnerships. Secure by design.
Reducing site burden at its finest
HumanTrue helps clinical sites work smarter, automating protocol interpretation, optimizing regulatory workflows, and accelerating study operations. Sites can launch faster, reduce errors, and align more easily with CROs and sponsors, all while maintaining HIPAA and SOC 2 compliance. With centralized access to study details, teams stay informed, efficient, and ready to move.
We help sites...
Maximize Output, Minimize Effort
HumanTrue empowers clinical trial sites to operate more efficiently, launch studies faster, and build stronger partnerships with CROs and sponsors. By automating manual tasks like protocol interpretation and regulatory document creation, the platform reduces preventable errors, improves consistency across teams, and saves valuable time. HumanTrue also reveals operational complexity early, equipping teams with feasibility and coverage insights before key commitments are made. Backed by HIPAA and SOC 2 compliance, it enables sites to maximize output with minimal effort without compromising on data security or regulatory standards.
Accelerate Study Start Times
Simplify site training and onboarding with a protocol expert that is available 24/7, saving time, confusion and frustration that comes with getting staff up to speed with the newest information. Reduced time for custom regulatory document delivery, allowing for quicker IRB submission and approval.
Bridge the Gap Between CRO Expectations and Site Execution
Align expectations from the beginning of the partnership with easy access to study details and requirements. Quicker and more open communication between key stakeholders with shared information all in one place.
Stay Secure and Compliant
Built with HIPAA and SOC 2 compliance at its core, ensuring all data is protected and private. Full traceability, documentation, and access logs to support regulatory readiness at any time. Built to meet the expectations of clinical partners and pass even the most rigorous vendor scrutiny.
How it Works
HumanTrue's AI application understands clinical trials, starting with the protocol. Our secure portal is where your team can interpret the study, understand its nuance, and produce operational content and manage processes.
First, Understand the Protocol
An undervalued aspect of managing clinical trials is understanding the trial. The problem is magnified with the more people involved. Stop searching PDF files manually, stop sending the wrong version over email. HumanTrue can manage your protocol in one place - including amendments - and transform it into an interactive portal.
In minutes of uploading the protocol, HumanTrue creates a study-specific report that includes all the key information you need to know about the study. For questions we didn't answer in advance there is chat - ask unlimited questions about the study and share answers with teammates.
ROI for CROs
Role:
PI
Responsibilities:
Overall responsibility for the conduct of the clinical trial at the site, ensuring adherence to protocol and regulations, subject safety, and data integrity.
Pain Point:
Oversight complexity
With HumanTrue:
Protocol-to-action clarity
Role:
CRC
Responsibilities:
Handles daily operations including patient recruitment, visit scheduling, data entry, and maintaining study documentation.
Pain Point:
Admin burden
With HumanTrue:
Automated docs, Simplifies eligibility criteria review
Role:
Regulatory
Responsibilities:
Prepares and submits IRB/ethics documents, ensures all study approvals and documents are current.
Pain Point:
Version control, submissions
With HumanTrue:
IRB-ready docs
Role:
Research Nurse
Responsibilities:
Conducts clinical assessments, collects samples, monitors participant safety, and ensures adherence to protocol procedures.
Pain Point:
Procedure overload
With HumanTrue:
Quick protocol key info extraction and interpretation
Role:
Data Coordinator
Responsibilities:
Enters and verifies clinical trial data in EDC systems and ensures accuracy and timeliness.
Pain Point:
Inconsistent documentation
With HumanTrue:
Standardized, source-linked clarity