Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
SiteCentric is an integrated platform designed for clinical trial management, specifically created by research sites to address their unique needs, which combines various functions such as CRM, eISF, CTMS, financial management, and reporting into one cohesive system. This comprehensive solution streamlines and automates processes throughout the entire trial lifecycle, facilitating the nurturing of study leads and organization of pipeline activities with a specialized CRM. It also centralizes essential documents, including budgets, contracts, eReg, training records, and source documentation, to ensure a swift startup process. Additionally, it enhances enrollment efforts through targeted outreach strategies and by utilizing existing databases for more effective recruitment. The platform tracks patient visits meticulously while capturing high-quality eSource data, and conducts internal quality control checks along with maintaining version control and audit-ready eISF documentation. Furthermore, it oversees financial aspects such as budgets, invoicing, payment reconciliation, and patient reimbursements, while also providing leadership dashboards that reveal key performance metrics and trends in real-time, allowing research sites to make informed decisions quickly. Ultimately, SiteCentric empowers research sites by consolidating various functionalities into one efficient platform tailored to enhance clinical trial operations significantly.
Description
TrialMind serves as an AI-driven clinical research platform catering to pharmaceutical and biotechnology firms, contract research organizations, and academic medical institutions. The platform's capabilities extend to trial design, statistical programming, real-world evidence generation, cohort analysis, literature reviews, and research into the clinical trial landscape, as well as supporting clinical operations. Its workflows encompass various essential processes such as site selection, matching patients to trials, refining eligibility criteria, forecasting enrollment and dropout rates, and conducting data and medical monitoring. Users can articulate their tasks using natural language, examine analysis plans, and review findings with connections to relevant sources, methodologies, and code. TrialMind is available in multiple formats, including hosted software, private cloud solutions, or deployment directly within a client's infrastructure. Importantly, raw patient records remain within the customer’s environment throughout the matching process, ensuring data privacy. Additionally, API and Model Context Protocol access facilitate the integration of its functionalities into other platforms, enhancing usability and efficiency. This comprehensive approach empowers research teams to streamline their clinical trials effectively.
API Access
Has API
No
API Access
Has API
Yes
Integrations
Model Context Protocol (MCP)
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Pricing Details
$500/user/month
$500 per user per month.
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
No
Live Rep (24/7)
Yes
Online Support
Yes
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
No
Types of Training
Training Docs
Yes
Webinars
No
Live Training (Online)
Yes
In Person
No
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
Yes
In Person
No
Vendor Details
Company Name
SiteCentric
Founded
2022
Country
United States
Website
sitecentric.com
Vendor Details
Company Name
Keiji AI, Inc.
Founded
2023
Country
United States
Website
keiji.ai
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
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