Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
KEI Project streamlines all project data and components into a single location, enabling rapid and effortless access for every team member. Why not start your Free Trial today? Our software is designed for quick and easy customization to meet your specific requirements. Should you need assistance, we will ensure you are operational at a highly competitive rate. Experience the advantages now by trying out our Free Trial. Additionally, KEI Project boasts an intuitive interface that allows seamless integration with KEI CRM if you're using it. It is straightforward to learn and can be implemented swiftly. With prices that are all-inclusive and highly competitive, it can be fully tailored to suit your business needs. Our web-based applications are accessible from any device with a web browser, and support is offered throughout North America, seven days a week. Regular updates, driven by customer feedback, are provided at no extra cost, and we offer guarantees—just ask us for more information. Moreover, for enhanced security, the system can be encrypted and is designed with role-based access controls to ensure your data remains protected.
Description
Clinical One RTSM is capable of accommodating various randomization strategies, ranging from the most straightforward to highly intricate studies, all without requiring any programming or coding, which consequently reduces the duration of user acceptance testing. You can take charge of your study with self-service configurations, allowing you to develop a study in just a matter of days rather than weeks. Additionally, you can assess the drug inventory status and make real-time adjustments without needing to consult the vendor, thereby avoiding unnecessary costs and change requests. By implementing changes swiftly, you can eliminate expenses associated with change requests and prevent delays, enabling you to launch your studies almost instantaneously. This platform stands out as the only one that genuinely integrates individuals, processes, and data to streamline and expedite the future of clinical trials. Moreover, the inclusion of virtual components in clinical trials enhances patient engagement and significantly elevates the quality of trial data. To keep pace with the rapidly evolving landscape, it is essential to adopt transformative digital strategies that facilitate quicker study initiations, harmonize data from diverse sources, and optimize workflow efficiency. Such advancements are pivotal for the successful execution of modern clinical research initiatives.
API Access
Has API
No
API Access
Has API
No
Integrations
Greenlight Guru Clinical
No
Pricing Details
$21 per month
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)
Yes
Online Support
Yes
Types of Training
Training Docs
Yes
Webinars
No
Live Training (Online)
No
In Person
Yes
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
Yes
In Person
Yes
Vendor Details
Company Name
KeiWare Software Applications
Founded
2011
Country
Canada
Website
www.keiwareapplications.com/Home/KeiProject
Vendor Details
Company Name
Oracle
Founded
1977
Country
United States
Website
www.oracle.com/life-sciences/clinical-trials/clinical-one-randomization-supplies-management/
Product Features
Project Management
Agile Methodologies
Yes
Budget Management
No
Client Portal
Yes
Collaboration Tools
Yes
Cost-to-Completion Tracking
Yes
Customizable Templates
Yes
Gantt Charts
Yes
Idea Management
Yes
Kanban Board
Yes
Milestone Tracking
No
Portfolio Management
No
Resource Management
No
Time & Expense Tracking
No
Traditional Methodologies
Yes
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