OpenClinica
OpenClinica is a unified clinical data management platform that provides electronic data capture, participant engagement, and automated reporting to accelerate the speed and improve the accuracy of clinical trials.
RealTime-CTMS
RealTime-CTMS is a comprehensive clinical trial management system designed to help clinical research sites, networks, and sponsors manage study workflows, patient recruitment, and financial tracking in one centralized platform.
Quick Comparison
| Feature | OpenClinica | RealTime-CTMS |
|---|---|---|
| Website | openclinica.com | realtime-ctms.com |
| Pricing Model | Custom | Custom |
| Starting Price | Custom Pricing | Custom Pricing |
| FREE Trial | ✘ No free trial | ✘ No free trial |
| Free Plan | ✓ Has free plan | ✘ No free plan |
| Product Demo | ✓ Request demo here | ✓ Request demo here |
| Deployment | ||
| Integrations | ||
| Target Users | ||
| Target Industries | ||
| Customer Count | 0 | 0 |
| Founded Year | 2004 | 2013 |
| Headquarters | Waltham, USA | San Antonio, USA |
Overview
OpenClinica
OpenClinica provides a unified environment to manage your clinical research data from start to finish. You can build complex studies quickly using a drag-and-drop interface, capture data electronically through intuitive forms, and engage participants directly via their own devices. The platform eliminates manual data entry hurdles by automating the flow of information from electronic health records directly into your study database.
You can maintain high data quality with real-time edit checks and automated queries that flag inconsistencies immediately. Whether you are running a small academic study or a large-scale global trial, the system scales to meet your regulatory compliance needs, including 21 CFR Part 11. It helps you reduce study timelines by providing instant access to clean, analysis-ready data through built-in reporting and visualization tools.
RealTime-CTMS
RealTime-CTMS provides you with a centralized hub to manage every aspect of your clinical research operations. Whether you are running a single site or a global research network, you can track study progress, manage complex protocols, and maintain regulatory compliance without juggling multiple spreadsheets. The platform focuses on eliminating administrative bottlenecks so your team can spend more time on patient care and data integrity.
You can streamline your entire study lifecycle from initial feasibility to final closeout. The software helps you manage patient recruitment databases, schedule participant visits with automated reminders, and handle intricate financial tracking including investigator payments and sponsor invoicing. By integrating your clinical and administrative workflows, you gain real-time visibility into your site's performance and financial health.
Overview
OpenClinica Features
- Electronic Data Capture Build and deploy web-based case report forms quickly with a user-friendly designer that requires no advanced programming skills.
- Participate (ePRO) Collect data directly from patients on their own smartphones or tablets to improve engagement and reduce site visits.
- Clinical Data Mart Access your study data in a flexible, relational format that makes it easy to create custom reports and visualizations.
- Data Integration Connect your study directly to electronic health records to pull clinical data automatically and eliminate manual transcription errors.
- Automated Queries Set up logic-based rules that automatically flag data discrepancies, allowing your team to resolve issues in real-time.
- Randomization Manage subject assignments and drug supply logistics within the same platform to ensure your study remains blinded and balanced.
RealTime-CTMS Features
- Patient Recruitment. Search and filter your entire participant database to identify eligible candidates for new studies quickly and efficiently.
- Study Scheduling. Manage complex visit windows and track participant attendance with automated text and email reminders to reduce no-shows.
- Financial Management. Generate sponsor invoices automatically and track investigator payments to ensure your site stays profitable and financially transparent.
- Regulatory Document Management. Store and track essential study documents in a secure environment to ensure you are always audit-ready.
- E-Source Integration. Capture clinical data electronically at the point of care to eliminate paper records and reduce transcription errors.
- Real-Time Reporting. Access instant insights into enrollment metrics, site productivity, and financial performance through customizable management dashboards.
Pricing Comparison
OpenClinica Pricing
RealTime-CTMS Pricing
Pros & Cons
OpenClinica
Pros
- Highly flexible form builder supports complex clinical protocols
- Strong compliance features for regulatory audits and security
- Active community support for the open-source edition
- Intuitive interface for site coordinators and data entry
Cons
- Self-hosted version requires significant technical expertise to maintain
- Advanced reporting features may require a learning curve
- Customization of complex workflows can be time-consuming
RealTime-CTMS
Pros
- Excellent financial tracking for complex sponsor invoicing
- Highly responsive customer support and implementation team
- Comprehensive patient recruitment and database filtering tools
- User-friendly interface compared to legacy CTMS platforms
Cons
- Initial system configuration requires significant time investment
- Advanced reporting features have a steeper learning curve
- Mobile functionality is more limited than the desktop version