Upload your study documents. MindBridge extracts, structures, and operationalizes them — so your team always works from the latest trusted knowledge.
Drop in protocols, ICFs, investigator brochures, SOPs, or any study-related document. MindBridge parses every format.
MindBridge reads your documents and extracts eligibility criteria, procedures, safety information, visit schedules, and key protocol details — each tagged with confidence scores.
Your team reviews extracted knowledge, tracks tasks through completion, manages visit schedules, and generates visit templates — all from one place.
MindBridge doesn't just store documents — it extracts, structures, and operationalizes them into role-specific knowledge your team can search, verify, and act on.
A living repository of extracted protocol knowledge — eligibility criteria, procedures, safety data, visit requirements — searchable, version-tracked, and always current.
When a protocol amendment arrives, upload and supersede. MindBridge shows exactly what changed — added criteria, modified procedures, removed rules — and flags any SOPs or templates that need regeneration.
Manage patient visits with a calendar view. Track visit windows, generate visit-specific document templates, and ensure no screening or follow-up falls through the cracks.
Walk through extracted inclusion and exclusion criteria per patient with a structured checklist. Track tasks, deviations, and findings across your study team with role-aware workflows.
Ask questions and get answers grounded in your actual study documents — with source citations and confidence scores. A 23-tool agentic system that searches, cross-references, and reasons across your protocol knowledge.
Manager, Contributor, and Viewer roles ensure the right people have the right access. Principal Investigators, coordinators, and study nurses each see what they need.
Whether you're running a single-center Phase III or coordinating across multiple investigators — MindBridge keeps your study knowledge organized and your team in sync.
Your study data stays in Europe. MindBridge is a coordination and knowledge tool — not a CTMS, not an EDC, and not a medical device.
All data stored in Supabase EU West (Ireland). Hosted on Vercel's Dublin region. Your data never leaves the European Union.
Full Data Processing Agreement available. Your institution is the Data Controller. MindBridge operates strictly as a Data Processor under GDPR Article 28.
Granular permissions with Manager, Contributor, and Viewer tiers. Every action is attributed to a user. Workspace isolation between studies.
Service agreement, DPA, sub-processor register, security documentation, and data residency confirmation — all prepared and ready for your institution's review.
Important: MindBridge Hub is a coordination and knowledge management tool for clinical research teams. It is not a Clinical Trial Management System (CTMS), Electronic Data Capture (EDC) system, or medical device. It does not replace regulatory-mandated clinical systems. It helps your team stay organized and access study knowledge faster.