One accountable path from trial operations to decision-ready data.
AIClinTrack brings sponsors and CROs a connected CTMS and eTMF foundation, backed by professional services in medical writing, clinical data management, and biostatistics.
- CTMS available
- eTMF foundation available
- EDC & IWRS in pilot
Product screen shown with synthetic sample data · click to enlarge
- Trial Design
- Protocol Development
- Medical Writing
- Clinical Data Management
- Biostatistics
- Statistical Programming
- CDISC SDTM & ADaM
- CTMS
- eTMF
- RBQM & QMS in CTMS
Software for visibility. Specialists for the work.
Use the platform where it is production-ready and engage our teams where people, process, and cross-system coordination matter most.
Clinical Trial Management System
Coordinate studies, sites, milestones, monitoring, risk, and quality workflows — with RBQM and QMS included.
- Study setup
- Site activation
- Monitoring
- Milestones
- RBQM Center
- QMS
- Audit history
- 01Set up study
- 02Activate sites
- 03Oversee monitoring
- 04Track & report
eTMF foundation
Essential documents with controlled versions, QC review, role-based access, and activity history.
Learn moreTrial design & medical writing
Study design input, protocols, ICFs, clinical study reports, lay summaries, and submission documents.
Learn moreClinical data management
System-agnostic support from CRF design and study build through cleaning and database lock.
Learn moreBiostatistics & programming
Statistical design input, SAPs, CDISC SDTM and ADaM datasets, and quality-controlled TLFs.
Learn morePilotEDC & IWRS— running as a pilot with selected studies.Learn about the pilotSee the product your teams will use
Real AIClinTrack screens — clear status, structured workflows, and the context each role needs to act.
Product screens shown with synthetic sample data. Click a screen to enlarge.
Continuity from protocol interpretation to clean-data handoff
A practical operating model keeps ownership visible and quality activities moving throughout the study — not only at close-out.
- 01
Plan
Translate protocol requirements into operational and data-management plans.
- 02
Build
Configure study workflows and support eCRF, database, edit-check, and UAT activities.
- 03
Conduct
Maintain oversight, review data, manage queries, reconcile sources, and monitor quality.
- 04
Close
Drive final review, database-lock readiness, controlled handoff, and archive support.
Clear status, governed access, and traceable work
AIClinTrack supports the controls and operating discipline clinical teams need while leaving final validation, quality, and regulatory decisions with authorized study personnel.
Quality by design
Risk-proportionate planning and oversight aligned to modern GCP principles.
Controlled access
Role-based access and tenant isolation for appropriate study visibility.
Traceable workflows
Activity history and structured follow-up across operational work.
Global collaboration
A shared operating view for distributed sponsor, CRO, and service teams.
Extend your team without losing oversight
Scope, systems, responsibilities, standards, and deliverables are agreed for each engagement — so you always know who owns what.
Full-study delivery
Hand us end-to-end data management or study operations with agreed standards, milestones, and governance.
Defined work package
Scope a specific deliverable — database build, cleaning sprint, TLFs, or a regulatory document — with clear acceptance criteria.
Embedded functional support
Extend your in-house team with experienced specialists working inside your systems and SOPs.
Build a clearer operating model for your next study
Tell us where your operational or data-management workload is creating risk, delay, or fragmented oversight.