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 multi-tool agentic system that searches, cross-references, and reasons across your protocol knowledge.
Study-level roles — Manager, Contributor, and Viewer — control what each team member can do. Clinical role labels like PI, Coordinator, and Study Nurse fine-tune permissions such as task review and visibility.
Whether you're running a single study or coordinating across multiple trials — MindBridge keeps your study knowledge organized and your team in sync.
MindBridge is a coordination and knowledge tool — not a CTMS, not an EDC, and not a medical device. Your data is hosted in the EU with full GDPR compliance.
EU-hosted infrastructure with role-based access control, workspace isolation between studies, and full data residency transparency. DPA available upon request.
Service agreement, sub-processor register, security documentation, and data residency confirmation — all available 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.