IRB-ready AI for sponsors, sites, and patients

From Protocol to Feasibility in Minutes.

Accelerate site identification and engagement with AI-generated, IRB-ready video summaries for Investigators, Site Staff, and Patients.

IRB & SOC-Ready ArchitectureTraceable AIAudit-Ready Logs

Workflow

From Protocol to Video in 3 simple steps

01

Upload protocol

Upload PDF, DOCX, paste text, review PowerPoint presentations, or collate important changes from emails.

02

Render & Edit Video

Generate a branded slide+narration video that is fully customizable. Edit the tone or emphasize key protocol points to fit your specific needs.

03

Track Engagement

Monitor how viewers interact with your content. Track video watch times, identify drop-off points, and monitor data interaction.

Protocol intelligence

Real-time answers — for sites and sponsors.

Every uploaded protocol becomes a private, auditable knowledge base. PIs ask questions and get answers in seconds. Sponsors see the questions sites are actually asking, and pre-answer them.

Protocol SME chat

A subject-matter expert grounded strictly in your protocol document. PIs and study coordinators ask anything — eligibility, dosing, schedule of assessments, safety reporting — and receive concise, cited answers in real time.

  • Source-bound. Never uses outside knowledge — only the uploaded protocol.
  • Hard escalation. Out-of-scope questions return a fixed handoff to the clinical lead.
  • Cuts site burden. Replaces back-and-forth email cycles with instant, auditable answers.
PI · 09:42
Can a patient on prophylactic anticoagulation be enrolled?
Protocol SME
Per Section 5.2 / Exclusion #4 — therapeutic-dose anticoagulation excludes; prophylactic low-dose LMWH is permitted with PI judgement.

Two-way FAQ generator

One click produces two grounded FAQs from the protocol — actionable insight for sponsors, operational answers for sites. Questions flow in both directions so neither side is guessing.

Sponsor / Pharma FAQ
  • · Feasibility & screen-fail risk
  • · Site burden signals
  • · Endpoint & timeline risks
  • · Likely PI questions to pre-empt
Investigator / Site FAQ
  • · Eligibility edge cases
  • · Dosing & administration
  • · Visit windows & assessments
  • · Safety reporting timelines

Pharma teams ship a study with answers already in hand. PIs onboard without waiting on a medical monitor. Both sides start aligned.

Built for trust

A communication tool, not a demo.

A communication tool, not a demo. Summit prioritises clarity, accuracy, and auditability over flashy visuals. Every video is branded to your protocol or need.

  • Role-based workspaces
    Fully customizable video delivery based on your audience (e.g., study nurse, PI, patient, or study team).
  • Engagement analytics
    Track specific viewer engagement, watch-through rates, and drop-offs.
Live preview · ONCO-204 Ph2
NCT05000000
Scene 03 · Endpoints
Primary endpoint: ORR at week 24
RECIST v1.1 · independent central review
0:42 / 3:18CDA required at 1:30
Views
128
CDA signed
42
Avg watch
78%

Designed with sponsors, CROs, PIs, and patients in mind.

Every Summit video is auditable end-to-end. Source protocol, generated script, rendered video, and viewer identity are linked in one record.