secuTrial
Electronic data capture (EDC) software
Life sciences software
Clinical research software
- Features
- Ease of use
- Ease of management
- Quality of support
- Affordability
- Market presence
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What is secuTrial
secuTrial is an electronic data capture (EDC) platform used to design, run, and manage clinical studies, including data collection via electronic case report forms (eCRFs). It is used by sponsors, CROs, academic research organizations, and study sites to support study setup, subject data entry, monitoring, and audit-ready documentation. The product is positioned for regulated clinical research and includes capabilities that extend beyond core EDC, such as safety and trial management modules depending on deployment. It is commonly deployed in environments that require controlled access, audit trails, and validation-oriented processes.
Regulated-trial governance features
secuTrial includes controls typically required in regulated clinical research, such as role-based access, audit trails, and structured study configuration workflows. These capabilities support inspection readiness and traceability expectations in GxP environments. It is designed to fit validation-oriented operating models where change control and documentation are important. This aligns with common requirements for sponsors and CROs running interventional trials.
Broad clinical study coverage
The platform supports a range of study types and operational models, including sponsor-led, CRO-managed, and academic studies. It provides configurable eCRFs and study workflows that can be adapted to different protocols and data collection needs. This flexibility can reduce the need to adopt multiple point tools for different study designs. It is relevant for organizations running multiple studies with varying complexity.
Modular eClinical capabilities
secuTrial is offered with modules that can extend beyond core EDC, depending on licensing and implementation, to support adjacent clinical operations. This can simplify integration and vendor management when an organization prefers a more consolidated stack. A modular approach also allows teams to adopt functionality incrementally. It provides an alternative to assembling separate systems for each clinical function.
Implementation can be resource-heavy
Study build, validation activities, and governance processes can require specialized expertise and time, particularly for complex protocols. Organizations without established clinical systems teams may rely more on vendor or partner services. This can increase total implementation effort compared with lighter-weight EDC tools. Timelines may be longer when extensive documentation and controlled configuration are required.
User experience varies by role
EDC platforms optimized for compliance and configurability can feel less streamlined for some site users than tools designed primarily for rapid data entry. Training needs may be higher for study teams working across multiple modules. Usability perceptions can vary depending on how the study is configured and the complexity of forms and workflows. This can affect adoption speed at sites with limited bandwidth.
Integration work may be needed
Connecting EDC to external systems (e.g., CTMS, ePRO/eCOA, labs, randomization, or data warehouses) often requires integration planning and technical effort. The degree of out-of-the-box connectivity depends on the specific environment and modules in use. Organizations with standardized enterprise integration patterns may still need custom interfaces or middleware. This can add cost and coordination across vendors and internal IT.
Seller details
interActive Systems GmbH
Berlin, Germany
1996
Private
https://www.secutrial.com/
https://www.linkedin.com/company/interactive-systems-gmbh
