Anju TrialMaster
Anju TrialMaster is a comprehensive electronic data capture solution designed to streamline clinical trial workflows by providing integrated tools for data collection, management, and real-time reporting.
Viedoc
Viedoc is a unified eClinical solution designed to accelerate clinical trials through integrated electronic data capture, trial management, and real-time data monitoring for life science researchers.
Quick Comparison
| Feature | Anju TrialMaster | Viedoc |
|---|---|---|
| Website | anjusoftware.com | viedoc.com |
| Pricing Model | Custom | Custom |
| Starting Price | Custom Pricing | Custom Pricing |
| FREE Trial | ✘ No free trial | ✘ No free trial |
| Free Plan | ✘ No 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 | 2002 | 2003 |
| Headquarters | Tempe, USA | Uppsala, Sweden |
Overview
Anju TrialMaster
TrialMaster is an electronic data capture (EDC) platform that helps you manage the complexities of clinical trials from phase I through IV. You can collect, manage, and analyze clinical data in a centralized environment that prioritizes regulatory compliance and data integrity. The platform eliminates manual paper processes by providing digital forms and automated validation checks to ensure your study data is accurate from the moment of entry.
You can improve your site productivity using the intuitive interface that supports multi-language entry and complex study designs. Whether you are running a small pilot or a global multi-center trial, the software scales to meet your needs with integrated modules for medical coding, risk-based monitoring, and eSource. It helps you reduce study timelines by simplifying the query management process and providing instant access to trial performance metrics.
Viedoc
Viedoc provides a unified platform to manage every stage of your clinical trials, from initial study design to final data reporting. You can replace fragmented systems with a single interface that handles electronic data capture (EDC), clinical trial management (CTMS), and electronic trial master files (eTMF). This integration helps you maintain data integrity while reducing the time spent on manual data entry and reconciliation across different providers.
The platform is built to scale with your research needs, whether you are running a small early-phase study or a complex global trial. You can manage patient-reported outcomes directly through mobile devices and use built-in coding and logistics tools to keep your study on track. By centralizing your clinical operations, you gain better visibility into trial progress and can make faster, data-driven decisions to bring new treatments to market.
Overview
Anju TrialMaster Features
- Intuitive Study Builder Create and deploy complex clinical studies quickly using a drag-and-drop interface that requires no advanced programming skills.
- Flexible eSource Integration Capture data directly at the point of care to reduce transcription errors and eliminate the need for manual data entry.
- Advanced Medical Coding Streamline your coding process with integrated MedDRA and WHODrug dictionaries that suggest terms automatically for faster processing.
- Real-time Data Validation Set up automated edit checks that flag inconsistencies immediately, ensuring you maintain high data quality throughout the trial.
- Mobile Data Access Access your trial data and perform site monitoring tasks from any location using the responsive mobile-friendly interface.
- Integrated Randomization Manage patient randomization and trial supply kits directly within the EDC workflow to keep your study moving forward.
Viedoc Features
- Viedoc Clinic. Capture and manage clinical data efficiently with an intuitive interface designed for site investigators and data managers.
- Viedoc Designer. Build your entire study workflow visually, including complex validation rules and forms, without needing advanced programming skills.
- Viedoc Me. Collect data directly from patients using their own devices to improve engagement and ensure high-quality primary outcomes.
- Viedoc Logistics. Manage your clinical supply chain and track investigational products from the warehouse to the patient in real-time.
- Viedoc TMF. Maintain a complete and compliant electronic trial master file with automated document filing and easy inspection readiness.
- Viedoc Reports. Monitor your trial performance with visual dashboards that highlight recruitment trends, data queries, and site productivity.
Pricing Comparison
Anju TrialMaster Pricing
Viedoc Pricing
Pros & Cons
Anju TrialMaster
Pros
- Highly flexible configuration for complex global study designs
- User-friendly interface reduces training time for site staff
- Excellent regulatory compliance features for FDA and EMA standards
- Strong reporting tools provide clear visibility into study progress
Cons
- Initial study setup can be time-consuming for new users
- Custom reporting requires a slight learning curve to master
- Pricing is less transparent than smaller entry-level EDC tools
Viedoc
Pros
- Highly intuitive interface reduces training time for site staff
- Fast study setup compared to traditional legacy EDC systems
- Excellent mobile experience for patient-reported outcomes
- Unified platform eliminates the need for complex third-party integrations
- Responsive customer support with deep clinical industry expertise
Cons
- Custom pricing makes it difficult for quick budget planning
- Advanced reporting features may require a learning curve
- Limited flexibility for highly unconventional non-clinical workflows