Accelerate Your Clinical Trials with Dream Trials CTMS
A unified, AI‑enabled platform that centralizes enrollment, site management, budgeting, and compliance—so you can bring therapies to market faster.
What is Dream Trials CTMS?
Dream Trials CTMS is a Clinical Trial Management System built to streamline every operational aspect of a study—from site activation and subject tracking to financial oversight and regulatory compliance. By consolidating data into a single, cloud‑based hub, it eliminates silos, reduces manual entry, and provides real‑time visibility for sponsors, CROs, and research sites
E-Consent
Secure and easy digital consent forms for participants.
Compliance
Meets HIPAA, GDPR, GxP, and CFR Part 11 standards.
Integration
Effortlessly connects with existing EHR/EMR systems.
Unlike legacy spreadsheets or fragmented tools, Dream Trials CTMS offers a unified data architecture where information entered once flows automatically across all modules (e.g., EDC, eTMF, RTSM)
Core Features
Unified Study Dashboard
Live metrics on enrollment, site activation, milestones, and budget spend.
Central contracts, training logs, performance scores, and visit scheduling.
Automated reminders, eligibility screening, and adherence monitoring.
Site & Investigator Management
Subject Tracking & Visit Scheduling
Financial Management
Budget creation, expense tracking, automated invoicing, and forecast vs. actual reporting.
Regulatory & Compliance Tools
eTMF, eCRF integration, audit trail generation, deviation tracking, and inspection‑ready.
Secure, Cloud‑Based Architecture
Role‑based access, GDPR/21 CFR Part 11 compliance, and regular penetration testing.
Included Modules
Specializing in clinical trial management solutions for sites.
eSource
Streamline data capture with seamless electronic source integration.
eConsent
Simplify patient consent with secure, easy-to-use electronic forms.
Manage training and documentation efficiently within one platform.
Training
FAQs
What is eSource?
eSource is electronic data capture directly from clinical sites, improving accuracy and efficiency.
How does eConsent work?
Can Dreamit2 integrate with EDC?
What training documentation is managed?
Are ISF documents supported?
eConsent allows patients to review and sign consent forms digitally, streamlining enrollment.
Yes, Dreamit2 seamlessly integrates eSource data with your existing Electronic Data Capture systems to ensure smooth data flow.
We handle all training documents, ensuring site staff have easy access to up-to-date materials for compliance.
Yes, our solution manages Investigator Site Files electronically for better organization and access.
Contact Us
Reach out for tailored clinical trial management solutions.
