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What is Clindata Cloud?

Clindata Cloud consolidates pre-clinical, clinical, and Risk Metric information from diverse sources, delivering clinical operations teams with ready-to-submit data sets, complete with analytics and alerts for risk-based monitoring. By integrating and harmonizing study data from various origins into a singular data model, it guarantees that incoming information undergoes validation for elements like completeness, accuracy, integrity, and consistency, while also issuing alerts for any detected anomalies or risk indicators. The data is standardized in accordance with CDISC data standards, which minimizes extraneous noise and streamlines the generation of real-time, ready-to-submit data sets, enabling continuous validation and analysis. Furthermore, it offers real-time analytics derived from the standardized data, providing crucial insights for clinical decision-making in a timely manner. This holistic approach not only improves the efficiency and reliability of clinical operations but also empowers teams with the tools needed for proactive risk management. Consequently, Clindata Cloud stands as a vital resource in enhancing the overall quality of clinical research.

What is CTMS Master?

CTMS Master stands out as the leading clinical trial management system, crafted to tackle the intricate technical issues associated with managing clinical trials. By enhancing user communication, minimizing manual tasks, and eradicating redundant data, CTMS Master streamlines the overall trial process. This system not only improves efficiency but also features a Site Visit Report tool that works seamlessly with an automated workflow to avoid any duplicate data entry. Additionally, it simplifies the generation and distribution of ready-to-use Site Visit Reports (SVR). Users can utilize standard templates for various documents related to sites and projects, including budgets, events, milestones, and reports on site visits. With CTMS Master, you gain access to over 100 metrics and statistics designed to monitor clinical study sites, countries, and projects effectively. Furthermore, it comes equipped with more than 80 standard reports and offers ad-hoc reporting options for customized insights. Users can also develop site-specific budgets based on a default template, track both accrued and future obligations, and establish either automatic or manual approval processes for each payment type, ensuring thorough financial oversight throughout the trial. This comprehensive approach not only enhances transparency but also fosters better decision-making in clinical trial management.

Media

Media

Integrations Supported

TrialMaster

Integrations Supported

TrialMaster

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

Clinical Data

Company Website

www.clindatainc.com

Company Facts

Organization Name

Anju Software

Date Founded

2016

Company Location

United States

Company Website

www.anjusoftware.com/ctms

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

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