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What is Clinion CTMS?

The Clinion Clinical Trial Management System (CTMS) offers an intuitive interface that integrates effortlessly with Clinion EDC and Clinion RTSM, providing rapid and thorough access to all elements of the trial process, thereby managing critical aspects such as investigator sites, patient enrollment, serious adverse events (SAEs), protocol deviations, participant inclusions, visit scheduling, investigational product (IP) management, key milestones, financial oversight, custom reporting, and real-time analytics, which collectively enhance quality, mitigate risks, and lower expenses. Designed with a modular architecture, Clinion CTMS includes a variety of modules tailored for specific needs, such as the Admin Module, Project Management, Site Monitoring Activities, Finance and Budget Management, Safety Reporting, IP Inventory Management, Document Management System, Audit/Activity Log, and provides comprehensive dashboards and reports to facilitate efficient trial oversight.

What is Citeline?

Citeline acts as a comprehensive platform for intelligence and analytics in clinical development, providing life sciences companies with essential real-time data, insights, and tools necessary for making well-informed strategic decisions throughout the drug and device development journey. By gathering and refining an extensive array of datasets concerning global clinical trials, investigators, trial sites, drug development pipelines, and regulatory requirements, it supports multiple functions, including protocol design, feasibility studies, site and investigator selection, enrollment forecasting, competitive analysis, and adherence to disclosure regulations across various regions. The platform features a variety of products, such as Pharmaprojects for tracking drug pipelines, Trialtrove for benchmarking clinical trials, Sitetrove for acquiring site and investigator information, Global Patient Insights to ensure feasibility matches actual patient access, and TrialScope Intelligence/Disclose to navigate the intricacies of regulatory disclosure mandates. Citeline’s diverse functionalities make it an indispensable asset for organizations seeking to optimize their clinical development workflows and improve their strategic decision-making processes. Furthermore, the seamless integration of these tools not only enhances efficiency but also equips organizations to adeptly handle the challenges associated with clinical trials and regulatory compliance in a constantly changing environment. This adaptability is crucial for maintaining competitiveness and ensuring successful outcomes in the fast-paced life sciences sector.

Media

Media

Integrations Supported

Clinion EDC

Integrations Supported

Clinion EDC

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

Clinion

Date Founded

2000

Company Location

India

Company Website

www.clinion.com/clinical-trial-management-system/

Company Facts

Organization Name

Citeline

Company Location

United States

Company Website

www.citeline.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

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