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HumanTrue Study Assistant

Your study knowledge base, available to every authorized role.

HumanTrue Study Assistant is the role-aware interface to the governed knowledge base for the study. It turns connected study evidence into fast answers and structured views that can be checked against their source, version, and review status.

Inside the Study Assistant

The assistant is the interface. The knowledge base is the foundation.

Move between study summaries, eligibility, populations, the Schedule of Activities, risks, benefits, procedures, and source content while the underlying knowledge remains structured, versioned, and governed.
  • Study information is organized for fast review.
  • Questions stay connected to the study in view.
  • Source content remains available for verification.
HumanTrue Study Assistant showing structured study information and protocol questions
Illustrative product view using demonstration study data. The application is available only within authorized customer environments.

Protocol intelligence for every role

Find the answer without losing the evidence.

The Study Assistant helps teams understand what the study requires, why it requires it, and where that requirement came from.

  • Evidence-linked answers

    Move from a plain-language answer to the protocol section, table, criterion, footnote, or supporting artifact behind it.

  • Structured study views

    Navigate eligibility, Schedule of Activities, procedures, endpoints, assessments, arms, epochs, and operational dependencies.

  • Role-aware guidance

    Give clinical development, sites, data management, biostatistics, medical writing, and vendors the context each role needs.

  • Version and amendment awareness

    Keep answers aligned to the protocol version in use and identify what changed when an amendment is introduced.

  • Connected study knowledge

    Bring the protocol, investigator brochure, SAP, lab and operational materials, regulatory feedback, sponsor decisions, QA findings, and approved evidence into one governed knowledge layer.

  • Reviewable by design

    Retain source provenance, confidence, QA status, audit history, and optional expert consensus for higher-assurance use.

What teams ask

You ask the same questions, so automate them.

Your organization or your team members likely review protocols for the same thing, multiple times a day. Recruiters look at population details. Phlebotomists look for labs and specimen collection procedures. Medical writers look to understand benefits and risks.

Use HumanTrue to not only automate answers to these questions, but to provide a consistent way to quickly see these details across a library of studies.

Quick answers without the PDF overload

Stop wasting time manually searching through PDF files. HumanTrue understands protocols and also knows clinical research. We understand what it is you're looking for and generate insights within minutes of uploading a protocol.

  • Prepare for a study startup meeting by reviewing key details like phase, indication, number of participants, eligibility criteria, and the study goals.
  • Start a feasibility analysis by reviewing the schedule of activities.
  • Create a list of labs specified in the protocol and see if any parameters deviate from the standard.
  • Start your recruiting efforts by understanding the population characteristics and the specific indications studied.
  • Analyze patient burden by quickly looking at the number of clinic visits, procedures, and read the analysis of risks.

Useful from design through delivery

One study.Many questions.One governed knowledge base.

The same study knowledge supports faster decisions across teams while preserving the source, version, review status, and responsibility boundaries behind each answer.

  1. Clinical development

    Review design intent, eligibility, endpoints, estimands, procedures, and protocol assumptions.

  2. Study operations and sites

    Clarify visit requirements, windows, participant pathways, burden, training needs, and escalation points.

  3. Data and statistics

    Connect assessments and endpoints to data collection, analysis requirements, SAP development, and downstream specifications.

  4. Medical writing and content

    Reuse verified protocol content in ICFs, plans, study materials, translations, and amendment updates.

Controlled customer access

Product intelligence stays inside the governed environment.

This website explains the capability. It does not provide public access to the Study Assistant or customer study information.
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Enterprise controls

  • Study-level and role-based access controls.
  • Isolated customer environments.
  • No customer data used to train or fine-tune external models.
  • Traceable answers, review status, and audit history.

Start with one protocol

Find what your current process cannot see.

Request a Working Session