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Datacapt

by Datacapt · Since 2019
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ActiveAvailable globallyCloud
Quick facts
VendorDatacapt
Year launched2019
StatusActive
LocationLYON, Rhone 69009, FR
Countries servedGlobal
Languages2
IntegrationsN/A
Free tierN/A
Free trialYES
Contact salesN/A

About Datacapt

Datacapt is a clinical data management software from Datacapt that securely manages the clinical data for studies, trials, and medical research. It provides customized solutions, real-time data access, and reliable reporting tools so researchers can efficiently analyze and share information. Datacapt's platform is designed to cater to various study requirements, ensuring compliance with industry standards while adapting to specific needs. The software supports integration with other data sources, improves collaboration among study teams, and facilitates data entry and validation processes. Key capabilities: secure data storage real-time reporting integration with external systems customizable workflows compliance tracking Best for: researchers and organizations that need a reliable solution for clinical trial data management.

Datacapt is a cloud-based electronic data capture (EDC) software designed to streamline the collection, management, and analysis of clinical trial data. Aimed at clinical research organizations (CROs), sponsors, academic researchers, research sites, and patients, Datacapt helps manage large volumes of data in a secure, efficient, and user-friendly environment. The software is built to enhance data quality, reduce errors, and improve the overall efficiency of clinical trials, with its core features including real-time data validation, automated data cleaning, and customizable reporting tools. The user interface of Datacapt is designed to be clean, simple, and intuitive, making it accessible for users with varying levels of technical expertise. Upon logging in, users are greeted with a dashboard that provides an overview of ongoing trials, along with key metrics and important data points. The navigation is straightforward, allowing users to quickly access study setup, data entry forms, and reporting tools. One of the software’s standout features is its customizable interface.

Pros & Cons

Pros
  • Ease of Use: This is a major recurring theme. Reviewers find the platform easy to design forms with, simple to use, and user-friendly for data entry personnel. The interface is described as "light" and straightforward.
  • Easy Setup and Deployment: The platform is reported to be easy to install and deploy, with a smooth testing process.
  • Excellent Customer Support: Customer support is consistently praised as "top" and very helpful. The company is seen as responsive and addressing requests promptly.
  • Fast and Efficient: Tasks can be completed quickly, and the platform contributes to efficient data collection, especially in multi-center studies. It helps reduce the time spent on correction processes.
  • Flexible Design: The form design is flexible and easy to adapt to study needs.
Cons
  • Missing Features: Lacks some features like tables, better handling of repeated data, and single-field monitoring.
  • Slow Conditional Logic: Minor delay when using conditional logic in forms.
  • PROs/eConsent Issues: PRO management and eConsent (especially for children) need improvement.

Features

Key features

EDC (Electronic Data Capture)

Core offering, emphasizing modern and compliant data collection.

eCRF (Electronic Case Report Form)

Tool for designing and managing electronic case report forms.

eSource

Enables direct data capture at the source.

eConsent

Facilitates electronic informed consent processes.

ePRO/eCOA (Electronic Patient-Reported Outcomes/Clinical Outcome Assessments)

Allows for electronic data collection from patients.

eConsult & Televisits

Supports remote patient interaction and decentralized trials.

CTMS (Clinical Trial Management System)

Provides tools for managing various aspects of clinical trials, especially for sites.

Decentralized Clinical Trials (DCT) Support

Platform designed to accommodate DCT models.

Modular and Flexible

Emphasized as adaptable to different study needs.

Easy to Use

Modern and intuitive interface.

Global Reach

Supports multiple languages and countries.

Secure and Compliant

Adheres to relevant regulations (GDPR, FDA 21 CFR Part 11, HDS, ISO 27001).

Real-time Reporting

Offers real-time monitoring and reporting capabilities.

Additional features

Form Builder

Tool for creating custom forms (eCRF, ePRO, eConsent).

Data Collection

Captures clinical trial data electronically.

Data Management

Manages and organizes collected data.

Data Monitoring

Allows for real-time monitoring of data.

Reporting & Analytics

Provides tools for generating reports and analyzing data.

Patient Management

Helps manage patient information and interactions.

Recruitment Automation

Automates aspects of patient recruitment.

Payment Processing (for Sites)

Simplifies payment processes for clinical trial sites.

Study Design

Supports the design and setup of clinical trials.

Collaboration

Likely facilitates collaboration among study stakeholders (though not explicitly stated).

Customization

Offers flexibility to tailor the platform to specific study requirements.

Scalability

Can be used for both small and large projects.

Multilingual Support

Supports 85+ languages.

Global Accessibility

Available in 45+ countries.

Integrations

While not specified, modern eClinical platforms often integrate with other systems.

Training and Support

Implied through the "Request Demo" and "Try for Free" options.

Security Features

Includes security measures to protect data (GDPR, FDA 21 CFR Part 11, HDS, ISO 27001 compliance).

Pricing

Free trial
Free version
Request a quote
Promo Offer

Monthly plans

Starting At
EUR 269/mo
billed monthly

Countries & Languages

Global
Countries served
2
Interface languages
20
Billing currencies

Interface languages

EnglishFrench

Billing currencies

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

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