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HumanTrue for research sites

Give every site team the study knowledge it needs.

Turn the protocol and supporting materials into one governed, source-linked workspace for startup, training, participant support, and day-to-day execution.

Reduce site burden

Less searching. Fewer preventable interpretation gaps.

HumanTrue makes protocol requirements easier to understand and reuse without exposing the simulator or customer environments through the public website.

  • Faster startup

    Prepare teams with study-specific answers, checklists, training, and operational content derived from governed study knowledge.

  • Stronger partnerships

    Align sponsor, CRO, and site expectations with the same source-linked definitions, decisions, and approved materials.

  • Controlled access

    Use role-based permissions, audit trails, and isolated study environments designed for enterprise clinical workflows.

    Review trust and security

From source to site

One study knowledge base supports the work.

HumanTrue can connect the protocol with the investigator brochure, lab manual, informed consent materials, operational guidance, decisions, and amendments. Teams ask questions and create approved materials without repeatedly interpreting disconnected files.
  • Study Assistant with source citations
  • Eligibility, visits, procedures, and Schedule of Activities
  • ICFs, screeners, training, and patient materials
  • Amendment impact and version-aware guidance
  • Human review and documented resolution where required

Built around site roles

Useful answers for the people running the study.

  • Principal investigator

    Protocol-to-action clarity

    Common burden: Oversight complexity

  • Clinical research coordinator

    Eligibility, visits, and documents in one place

    Common burden: Administrative burden

  • Regulatory

    Source-linked, IRB-ready content

    Common burden: Version control and submissions

  • Research nurse

    Study-specific procedure and safety guidance

    Common burden: Procedure overload

  • Data coordinator

    Standardized, traceable study knowledge

    Common burden: Inconsistent documentation

Operational confidence

Traceability stays with the answer.

A study team can move from an answer or generated artifact to the protocol passage, supporting source, rule, review decision, and version that produced it.

Understand before action

HumanTrue surfaces what needs a sponsor decision and preserves the approved interpretation for downstream teams.

Site partnership

Start with one study and one site workflow.

Discuss a Site Workflow