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HumanTrue for sponsors

Build institutional knowledge one governed study at a time.

Connect clinical development, biostatistics, study startup, data management, and vendors to one governed, source-linked knowledge base for the trial.

Across the development lifecycle

Make every downstream team faster by improving the source.

  • Clinical development

    Pressure-test design decisions

    Surface conflicting requirements and compare protocol scenarios before finalization.

  • Quality by design

    Make risk visible

    Turn ambiguity, operational dependencies, burden, and failure paths into reviewable evidence.

  • Biostatistics

    Connect endpoints to analysis

    Maintain continuity from protocol definitions and estimands through SAP and analysis metadata.

  • Study startup

    Generate from governed knowledge

    Accelerate ICFs, screeners, training, registries, and system inputs without silent drift.

Configure what already exists

A sponsor pilot applies the platform to your knowledge.

HumanTrue already supports protocol assurance, QA'd USDM, governed study knowledge, executable simulation, and downstream generation. A pilot configures and evaluates these capabilities using the sponsor's standards, costs, sites, and operating experience.
  • Protocol integrity and exception report
  • USDM 4.0 conformance, fidelity, and Schedule of Activities checks
  • Executable model and scenario comparison
  • Traceability and reproducibility evidence
  • Downstream output demonstration

  • Prospective

    Surface and resolve design questions before the study is built.

  • Historical

    Connect prior study evidence and compare modeled ranges with observed outcomes.

  • Parallel

    Run HumanTrue alongside the current process and compare outputs.

  • Portfolio

    Build reusable knowledge across studies, indications, assets, and protocol generations.

ROI for sponsors

Enable your partners, reduce costs.

Innovation lives in the details. Support shared understanding among CROs, sites, and participants.
Time to produce study deliverables with and without HumanTrue
DeliverableTraditional processWith HumanTrueImpact
Informed Consent Drafting2-3 days10-30 minutes90%+ time savings
Site Training Guides3-5 days< 1 hour95% time savings
Patient Screener2 days< 30 minutes85% time savings
ISO 17100 Content Translation3-4 weeks5-7 business days~75% time savings

From study knowledge to institutional knowledge

Build a clinical study knowledge base.

Historical protocols can be connected with investigator brochures, SAPs, lab manuals, operational materials, regulatory feedback, study decisions, and actual performance. Across studies, that knowledge becomes reusable by asset, indication, development program, and protocol generation.

A calibrated implementation

With sponsor-specific costs, indication experience, preferred-site data, and actual performance, HumanTrue can calibrate simulation and downstream workflows to the sponsor's operating environment. The implementation applies the existing platform rather than funding development of a new one.

Sponsor pilot

Bring one protocol and one decision that matters.

Discuss a Sponsor Pilot