Faster screenings
We’re engineering yes/no checklists tied to source clauses so coordinators can finish eligibility prep in hours, not days.
AI-powered clinical trial intelligence
Turn 400-page protocols into site-ready playbooks.
ProtocolIQ’s guarded AI agents ingest any clinical trial protocol, cite their sources, and output eligibility checklists, dosing cards, visit calendars, and safety briefs coordinators can trust.
Trial workspace
Phase III – CRC-201
Ready
Eligibility checklist published
Visit calendar
Safety alerts
- Grade 3 neuropathy → hold + dose -20%
- QTc > 500ms → notify PI, EKG repeat
- SAE reporting window: 24h
Impact we’re building
Designed to lift the load on coordinators, CRAs, and sponsors.
ProtocolIQ aims to replace manual hunting with structured, shareable knowledge so every stakeholder can stay ahead of protocol demands.
Clearer dosing
Dose adjustments, safety actions, and escalation paths will surface instantly—no more scavenger hunts through PDFs.
Aligned teams
Sponsors, CROs, and sites will work from the same living protocol source with updates captured in one audit trail.
Why ProtocolIQ
Give every site the same, unambiguous protocol guidance.
Guardrailed AI and deterministic QA translate dense trial documents into structured tools with source citations, so coordinators, investigators, and CRAs stay aligned and inspection-ready.
Site-ready summaries
AI-generated eligibility, dosing, visits, endpoints, and safety extracts arrive with citations and reviewer notes so teams can trust every field.
Deviation defense
AI guardrails highlight edge cases, dose modifications, and reporting deadlines before a violation can occur.
Coordinated workspaces
Role-based access, audit history, and exports connect sponsors, CROs, and sites without chasing edits across inboxes.
Product capabilities
ProtocolIQ delivers structured intelligence for every protocol component.
Protocol ingestion
Upload native or scanned PDFs. NLP + OCR extract key sections, ready to reconcile with source citations.
Eligibility intelligence
LLM-assisted normalization turns inclusion/exclusion text into yes/no screening rules and pre-screen forms with deterministic guardrails; export to CSV or REDCap instantly.
Visit calendar engine
Sequence-aware AI maps timepoint × procedure matrices, applies arm filters, and syncs to Outlook, Google, or PDF.
Safety & amendments
AI flags dose modification triggers, AE management rules, and highlights diffs across protocol versions with source traceability.
Workflow
From protocol upload to coordinated site execution in four steps.
ProtocolIQ stitches together ingestion, QA, publication, and monitoring so every stakeholder works from the same source of truth.
01
Upload & parse
Drop the protocol PDF; AI extracts eligibility, arms, visits, endpoints, and safety sections automatically.
02
Review & QA
Editors reconcile AI-cited outputs, lock in determinations, and route for approval with full audit tracking.
03
Publish to sites
Share interactive checklists, calendars, and dosing cards with coordinators via secure SSO login.
04
Monitor & update
Track clarifications, push amendments, and highlight what's changed so sites stay aligned instantly.
AI you can trust
Built for explainability, validation, and enterprise security.
ProtocolIQ layers proven large language models with transparent citations and review workflows so teams gain speed without compromising oversight.
Citation-first outputs
Every extraction anchors back to the protocol clause it came from, giving coordinators evidence in one click.
Clinical review workflows
Operational leads validate AI-generated summaries before publication, capturing approvals and change notes for the audit trail.
Enterprise safeguards
SSO, audit logging, and encrypted storage keep sensitive trial data protected while giving regulators the evidence trail they expect.
Talk to us
Partner with our product team to deploy ProtocolIQ Summarizer.
Share your top protocol pain points and we’ll map an onboarding plan across sponsors, CROs, and research sites.