HumanTrue for CROs
Win on speed without multiplying hidden ambiguity.
Turn every awarded protocol into governed operational knowledge, a faster startup package, and a differentiated sponsor experience.
Commercial advantage
Make protocol intelligence part of the delivery model.
HumanTrue gives a lean team the repeatable rigor of a specialist department across studies, therapeutic areas, and sponsor formats.
Faster startup
Generate study-specific documents, training, specifications, and structured data from one governed model.
Protected margins
Reduce repetitive interpretation, manual reconciliation, and amendment-driven rework.
Partner-grade evidence
Deliver provenance, QA status, exception handling, and audit-ready traceability with each output.
Lean teams, specialist rigor
Staff your trial like you have a blank check.
HumanTrue gives a lean team the roster of a global sponsor. Every protocol, site, and amendment runs through the same verified semantic model - so a handful of people get the rigor that used to take a department of specialists, on every protocol, ICF, IRB submission, and amendment alike. The expertise doesn't have to scale with your headcount. It's already built in.
- Per-protocol QA at scale. AI-assisted verification built-in; human certified review available.
- Operational services. No internal build needed. You get protocol verification, amendment governance, and startup-package generation from day one.
- From submission to site. Everything from regulatory filings to site-executable materials is produced from one verified semantic model, with full provenance on every output.
- Speed-to-activation. Coherent protocols mean faster activation and far less avoidable cost.
- Partner-grade trust. CRO integrations, IRB references, and source in every output. The deliverable a sponsor partner expects.
From RFP to active study
Reuse the work instead of restarting it.
Begin protocol review during the proposal process, preserve the structured study model after award, and expand it into the operational workspace.
- Permissions separate sponsors, studies, contractors, and third-party vendors.
- RFP analysis can transition into the awarded study without duplicating setup.
- Enterprise oversight spans studies while study teams see only assigned work.
- Exportable integrity reports and checklists support governed internal processes.
ROI for CROs
Increase your margins and reduce timelines.
| Deliverable | Current process | With HumanTrue | Time savings | Cost impact |
|---|---|---|---|---|
| Informed Consent Drafting | 2-3 days | 10-30 minutes | 90%+ | Equivalent cost, faster delivery |
| Site Training Guide Development | 3-5 days | < 1 hour | 95% | Staff capacity preserved |
| Patient Screener Development | 2 days | < 30 minutes | 85% | Faster recruitment start |
| Clinicaltrials.gov Summary | 1-2 days | 15-20 minutes | 90% | Improve registry quality |
1 source
Shared protocol intelligence for every study team.
Role-aware answers, source citations, structured views, shared study knowledge, and reusable checklists help teams stay aligned without adding meetings.
CRO partnership