Datatrak CTMS logo

Datatrak CTMS

by DATATRAK · Since 1996
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ActiveAvailable globallyCloud
Quick facts
VendorDATATRAK
Year launched1996
StatusActive
LocationCleveland , OH
Countries servedGlobal
Languages2
IntegrationsN/A
Free tierN/A
Free trialN/A
Contact salesYES

About Datatrak CTMS

Datatrak CTMS is a clinical trial management system from DATATRAK that supports the management and execution of clinical trials. It provides features such as study planning, subject management, and data collection so users can effectively monitor trials and ensure compliance with regulatory standards. The platform includes tools for real-time reporting and analytics, allowing researchers to access critical data quickly. Datatrak CTMS is designed to improve collaboration between study teams and simplify the trial process, ultimately helping organizations reduce costs and timelines. Key capabilities: study planning subject management data collection real-time reporting regulatory compliance Best for: clinical research organizations that need to manage multiple clinical trials efficiently.

Datatrak CTMS is a versatile software solution designed to streamline and optimize the management of clinical trials. Its standout features include a user-friendly interface, robust core functionalities, and seamless integration capabilities. The user interface of Datatrak CTMS is intuitive and easy to navigate, making it simple for users to access the information they need quickly and efficiently. The design elements are clean and modern, enhancing the overall user experience and ensuring that users can focus on their tasks without unnecessary distractions. One of the core functionalities that sets Datatrak CTMS apart from its competitors is its innovative approach to data management. The software is able to handle large datasets and complex operations with ease, providing users with the tools they need to analyze, track, and report on their clinical trial data effectively. In terms of performance, Datatrak CTMS is fast, efficient, and reliable. Users can trust that their data is secure and accessible at all times, even when working with massive amounts of information.

Pros & Cons

Pros
  • Comprehensive suite of tools for clinical trial management.
  • User-friendly interface enhances usability.
  • Integrated IWRS and coding systems streamline processes.
  • Risk-Based Monitoring capabilities improve data quality.
  • Supports both electronic and paper-based studies.
Cons
  • Limited publicly available information on support options.
  • Pricing details are not disclosed.
  • Specifics on language support are lacking.
  • Integration capabilities with other systems are not detailed.
  • Information on in-app marketplace availability is not provided.

Features

Key features

Intuitive User Interface

User-friendly design facilitating easy navigation and data entry.

IWRS (Interactive Web Response System)

Manages patient enrollment, eligibility, randomization, and study drug supplies seamlessly.

Query Management

Allows creation and management of queries to sites for efficient data clarification.

Coding

Built-in dictionaries (e.g., WHO-DD, MedDRA) for efficient coding of drugs and terms.

Risk-Based Monitoring (RBM)

Facilitates targeted monitoring strategies to enhance data quality and patient safety.

Additional features

Intuitive User Interface

Streamlines data collection with alerts and single sign-on capabilities.

IWRS

Integrates patient management and drug assignment within the platform.

Query Management

Enables efficient communication between sites and sponsors.

Coding

Automates manual coding activities with synonym capabilities.

Local Lab Lookup

Manages local lab ranges to determine abnormal values.

Import/Export

Allows on-demand data import and export, with scheduling and automation options.

Double Data Capture (DDE)

Supports conventional paper-based studies with built-in double data entry and comparison tools.

Risk-Based Monitoring (RBM)

Provides out-of-the-box functionality for SDV, data review, and eSignature.

Trial Design

Streamlines design-to-deployment using a single tool, reducing time to deployment.

eConsent/ePRO/eCOA

Offers cloud-based solutions for electronic consent and patient-reported outcomes.

Image Data Capture & Adjudication

Facilitates image data capture and adjudication within the platform.

CTMS

Integrates clinical trial management capabilities.

API

Provides application programming interfaces for system integration.

Pricing

Free trial
Free version
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Countries & Languages

Global
Countries served
2
Interface languages
18
Billing currencies

Interface languages

EnglishJapanese

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇯🇵JPY🇦🇺AUD🇨🇦CAD🇨🇭CHF🇨🇳CNY🇸🇪SEK🇮🇳INR🇷🇺RUB🇭🇰HKD🇳🇿NZD🇸🇬SGD🇰🇷KRW🇿🇦ZAR🇧🇷BRL🇲🇽MXN

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