Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
The platform features a sleek and user-friendly design, ensuring that navigation and data entry are both swift and effortless; it incorporates access control measures and SSL encryption for security, operates entirely online without the need for installations, and includes built-in monitoring alongside tools for data management and reporting, with a monthly flat rate (SaaS) that is customizable based on the size and duration of the study. Data collection is accelerated through an accessible web interface, allowing users to easily review the status of data completion with visual indicators, while it also employs edit checks and both automatic and manual queries to identify any discrepancies; additionally, it offers source data verification (SDV) and remote reviews through integrated buttons, meticulously tracking all changes made, including the author, date, time, and reason for each modification, and it can generate datasets (e.g., CSV) for subsequent statistical analysis, providing a comprehensive solution for research needs. This robust functionality ensures that users can efficiently manage their data while maintaining high standards of accuracy and security throughout the research process.
Description
Enhance the quality of data management by directly capturing eSource data during patient interactions. This process incorporates integrated editing and validation mechanisms, allowing users to electronically gather high-quality information, which significantly minimizes errors and inquiries, while facilitating real-time remote oversight. By doing so, the study duration, expenses, and risks are significantly reduced. FDA-endorsed, this innovative eSource approach simplifies and modernizes clinical trials, effectively replacing slow, error-prone monitoring and the transcription process into electronic data capture (EDC) systems. Additionally, tailored for site users, ez-SourceDocx optimizes workflows, alleviates workloads, and ensures adherence to study protocols by guiding sites through properly sequenced visit procedures, which not only confirm the collection of all endpoint data but also encourage timely quality assessments by investigators. Ultimately, this comprehensive system enhances overall clinical trial efficiency and reliability.
API Access
Has API
No
API Access
Has API
No
Integrations
ez-DIMS
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Types of Training
Training Docs
Yes
Webinars
No
Live Training (Online)
Yes
In Person
No
Types of Training
Training Docs
No
Webinars
No
Live Training (Online)
No
In Person
No
Vendor Details
Company Name
Sofpromed
Founded
2012
Country
Spain
Website
www.sofpromed.com
Vendor Details
Company Name
Alpha Clinical Systems
Founded
2009
Country
United States
Website
alphaclinicalsystems.com/ez-sourcedocx/
Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
Yes
Document Management
Yes
Electronic Data Capture
Yes
Enrollment Management
Yes
HIPAA Compliant
Yes
Monitoring
Yes
Patient Database
Yes
Recruiting Management
Yes
Scheduling
No
Study Planning
No
Product Features
Clinical Trial Management
21 CFR Part 11 Compliance
No
Document Management
No
Electronic Data Capture
No
Enrollment Management
No
HIPAA Compliant
No
Monitoring
No
Patient Database
No
Recruiting Management
No
Scheduling
No
Study Planning
No