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What is ez-SourceDocx?
Improve data management quality by capturing eSource data directly during patient encounters. This method includes integrated editing and validation features that enable users to collect high-quality information electronically, significantly reducing errors and inquiries while allowing for real-time remote monitoring. As a result, the overall duration, costs, and risks associated with studies are noticeably decreased. Approved by the FDA, this cutting-edge eSource method streamlines and modernizes the clinical trial process, effectively replacing traditional, error-prone monitoring and the manual transcription into electronic data capture (EDC) systems. Furthermore, designed with site users in mind, ez-SourceDocx enhances workflows, lightens workloads, and ensures compliance with study protocols by guiding sites through properly sequenced visit procedures, which not only guarantee the collection of all endpoint data but also promote timely quality evaluations by investigators. This all-encompassing system ultimately bolsters the efficiency and dependability of clinical trials while paving the way for innovations in data management practices. By leveraging technology in this manner, the potential for improved patient outcomes increases significantly.
What is SiteCentric?
SiteCentric is a comprehensive platform tailored specifically for clinical trial management, developed by research sites to meet their distinct requirements, integrating multiple functions like CRM, eISF, CTMS, financial oversight, and reporting into a single, cohesive solution. This all-encompassing tool simplifies and automates various processes throughout the entire lifecycle of a clinical trial, enabling effective management of study leads and the organization of pipeline activities through its specialized CRM system. Essential documents, such as budgets, contracts, eReg, training records, and source documentation, are centralized to streamline the startup process. Moreover, the platform boosts enrollment initiatives through strategic outreach and taps into existing databases for enhanced recruitment efficiency. Patient visits are meticulously tracked, ensuring high-quality eSource data is captured, while internal quality control checks, version control, and audit-ready eISF documentation are consistently maintained. Financial management is also a key feature, as it oversees aspects like budgets, invoicing, payment reconciliation, and patient reimbursements. The inclusion of leadership dashboards presents crucial performance metrics and trends in real-time, enabling research sites to make swift, informed decisions. Overall, SiteCentric significantly enhances clinical trial operations by consolidating various functionalities into a single, efficient platform, ultimately empowering research sites to achieve their goals more effectively while improving collaboration and operational efficiency.
Integrations Supported
ez-DIMS
API Availability
Has API
API Availability
Has API
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Company Facts
Organization Name
Alpha Clinical Systems
Date Founded
2009
Company Location
United States
Company Website
alphaclinicalsystems.com/ez-sourcedocx/
Company Facts
Organization Name
SiteCentric
Date Founded
2022
Company Location
United States
Company Website
sitecentric.com
Categories and Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning
Categories and Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning