Verial eTMF logo

Verial eTMF

by Triall · Since 2018
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ActiveAvailable globallyCloud
Quick facts
VendorTriall
Year launched2018
StatusActive
LocationBisonspoor 3002-C701, Copenhagen Tower 3605 LT, Maarssen, The Netherlands
Countries servedGlobal
Languages1
Integrations
Free tier
Free trial
Contact salesYES

About Verial eTMF

Verial eTMF is a clinical trial management software from Triall that delivers integrated technology and services for clinical trials. It combines ePRO/eCOA, eConsent, Virtual Visit, Wearable Integration, and Medical Coder so organizations can manage trial data efficiently. This software shortens study timelines and lowers costs while improving patient-centric services. Verial eTMF uses advanced technologies along with an industry-validated toolkit to support clinical operations effectively. Key capabilities: ePRO/eCOA eConsent Virtual Visit Wearable Integration Medical Coder Best for: clinical trial teams that need comprehensive management of clinical data and interactions.

Verial eTMF is a comprehensive software solution designed for managing electronic Trial Master Files (eTMF) in clinical trials. Standout features include its user-friendly interface, robust functionality, and seamless integration capabilities. The user interface of Verial eTMF is intuitive and easy to navigate, making it simple for users to access and manage their trial documentation. The design elements are clean and organized, enhancing the overall user experience and enabling efficient document management. One of the core functionalities that sets Verial eTMF apart from its competitors is its advanced search and indexing capabilities. Users can quickly locate specific documents or information within the system, saving time and improving workflow efficiency. Additionally, the software offers customizable dashboards and reporting tools, allowing users to track trial progress and performance effectively. In terms of performance, Verial eTMF excels in managing large datasets and complex operations. The software is fast, reliable, and capable of handling a high volume of documents without sacrificing speed or efficiency. This is essential for clinical trials, where accuracy and timeliness are paramount.

Pros & Cons

What users like
  • +Centralized Document Management: Streamlines the handling of clinical trial documents.
  • +Mobile Accessibility: Enables access from various devices and locations.
  • +Standardization: Utilizes the DIA TMF Reference Model for consistency.
  • +Auditability: Provides detailed audit trails for compliance.
  • +Compliance Assurance: Configurable permissions to maintain security and compliance.
What users flag
  • Limited Information on Integrations: Specific integration capabilities are not detailed.
  • Pricing Details Not Specified: Lack of publicly available pricing information.
  • Support Options Not Specified: Unclear what support channels are available.
  • Language Support Limited to English: May not accommodate non-English speaking users.
  • Mobile Accessibility Details Not Specified: Specifics on mobile platform compatibility are unclear.

Features

Key features

Document Management
Centralized platform for accessing, reviewing, editing, and signing trial-related documents.
Mobile Accessibility
Build and maintain the eTMF from virtually any device and location.
Site Engagement
Provides access to selected site staff members to promote engagement.
Standardization
Leverages prepopulated DIA TMF Reference Model folder structure.
Auditability
Verifiable and reportable audit trail logs of all user activity and document changes.
Compliance
Configurable role-based access permissions to ensure security and compliance.

Additional features

Document Management
Centralized platform for accessing, reviewing, editing, and signing trial-related documents.
Mobile Accessibility
Build and maintain the eTMF from virtually any device and location.
Site Engagement
Provides access to selected site staff members to promote engagement.
Standardization
Leverages prepopulated DIA TMF Reference Model folder structure.
Auditability
Verifiable and reportable audit trail logs of all user activity and document changes.
Compliance
Configurable role-based access permissions to ensure security and compliance.
Version Control
Automated version control to maintain document integrity.
Collaboration Tools
Real-time collaboration features for efficient document review and approval.
Reporting and Analytics
Tools for monitoring document status and ensuring inspection readiness.

Pricing

Free trial
Free version
Request a quote
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Countries & Languages

Global
Countries served
1
Interface languages
17
Billing currencies

Interface languages

English

Billing currencies

🇺🇸USD🇪🇺EUR🇬🇧GBP🇨🇭CHF🇯🇵JPY🇦🇺AUD🇨🇦CAD🇸🇪SEK🇳🇴NOK🇩🇰DKK🇳🇿NZD🇿🇦ZAR🇲🇽MXN🇸🇬SGD🇭🇰HKD🇮🇳INR🇨🇳CNY

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