---
description: Review of ACTide eCRF Software: system overview, features, price and cost information. Get free demos and compare to similar programs on Software Advice Ireland.
image: https://gdm-localsites-assets-gfprod.imgix.net/images/software_advice/og_logo-55146305bbe7b450bea05c18e9be9c9a.png
title: ACTide eCRF | Reviews, Pricing & Demos - SoftwareAdvice IE
---

Breadcrumb: [Home](/) > [Electronic Data Capture Software](/directory/4632/electronic-data-capture/software) > [ACTide eCRF](/software/560989/ACTide-eCRF)

# ACTide eCRF

Canonical: https://www.softwareadvice.ie/software/560989/ACTide-eCRF

> ACTide is a modular eClinical ecosystem designed to help CROs, pharmaceutical companies, biotechnology firms, medical device organizations, and research institutions manage clinical studies more efficiently, from study setup and data collection to monitoring, data cleaning, and reporting.&#10;&#10;Developed by Nubilaria, ACTide combines more than 20 years of experience in clinical data management with a flexible technological platform. Its modular architecture allows organizations to select the capabilities required for each study and expand the solution as their operational needs evolve.&#10;&#10;The ACTide ecosystem includes:&#10;&#10;• eCRF/EDC for secure and structured clinical data collection&#10;• Designer for independent study and database configuration&#10;• ePRO/eCOA for collecting patient-reported outcomes remotely&#10;• eTMF for organizing and controlling essential trial documentation&#10;• RTSM for randomization and clinical supply management&#10;• Safety tools for managing adverse events and safety workflows&#10;• CRA Tools for monitoring activities and source data verification&#10;• Data Manager Tools for validation, query management, and data cleaning&#10;• Project Management Tools for study oversight and coordination&#10;• Insight AI for natural-language data exploration, analysis, and reporting&#10;&#10;ACTide is built to support different operating models. Customers can configure and manage studies independently, collaborate with the ACTide team, or outsource selected activities such as database design, validation, data management, and study support. This makes the platform suitable both for organizations with established internal clinical operations and for teams that require additional expertise or resources.&#10;&#10;The system is designed for regulated clinical research environments and supports requirements and principles including ICH-GCP, GDPR, ISO Certifications, ALCOA+, CDISC/CDASH standards, and electronic record and signature controls. ACTide’s Validation Factory provides a structured approach to platform and release validation, helping customers reduce the effort required to maintain a controlled and inspection-ready environment.&#10;&#10;ACTide helps study teams address common operational challenges such as fragmented systems, manual processes, inconsistent data, delayed query resolution, limited study visibility, and complex vendor coordination. By bringing multiple clinical capabilities into one ecosystem, the platform supports greater data consistency and more efficient collaboration among sponsors, CROs, sites, monitors, data managers, and patients.&#10;&#10;Its configuration tools allow authorized users to create and update studies without depending entirely on vendor development cycles. Features such as field-level source data verification, visit signatures, multilingual capabilities, role-based access, audit trails, data exports, dashboards, and configurable workflows help teams adapt the platform to different protocols and study designs.&#10;&#10;ACTide Insight AI extends these capabilities by allowing authorized users to interact with clinical data through natural-language questions and generate real-time insights, dashboards, and exports. The objective is to make study information easier to access while keeping data governance, traceability, validation, and human oversight central to the process.&#10;&#10;ACTide can support clinical trials involving medicinal products, medical devices, and veterinary research across different phases and geographical locations. The platform is particularly suited to organizations seeking a long-term technology partner, a flexible implementation approach, and an alternative to rigid, disconnected clinical systems.&#10;&#10;Rather than offering software alone, ACTide combines technology, clinical data management expertise, validation services, and ongoing customer support. This collaborative approach helps organizations configure solutions around the real requirements of each study while retaining control over processes, data, and future platform evolution.
> 
> Verdict: Rated \*\*\*\* by 0 users. Top-rated for **Overall Quality**.

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## About the vendor

- **Company**: Nubilaria

## Commercial Context

- **Pricing Details**: For a free quotation, please contact our Sales Development Manager.
- **Target Audience**: 11–50, 51–200, 201–500, 501–1,000, 1,001–5,000, 5,001–10,000, 10,000+
- **Deployment & Platforms**: Cloud, SaaS, Web-based
- **Supported Languages**: English, French, German, Italian, Spanish
- **Available Countries**: Australia, Austria, Belgium, Canada, Czechia, Denmark, Finland, France, Germany, Hungary, Ireland, Italy, Netherlands, New Zealand, Norway, Poland, Portugal, Spain, Sweden, Switzerland and 2 more

## Features

- API
- Activity Dashboard
- Alerts/Notifications
- Approval Process Control
- Audit Trail
- CRF Tracking
- Clinical Study Management
- Compliance Management
- Configurable Workflow
- Customisable Forms
- Customisable Reports
- Customisable Templates
- Customizable Fields
- Data Capture and Transfer
- Data Extraction
- Data Import/Export
- Data Storage Management
- Data Verification
- Data Visualisation
- Digital Signature

## Support Options

- Email/Help Desk
- Knowledge Base
- Phone Support

## Category

- [Electronic Data Capture Software](https://www.softwareadvice.ie/directory/4632/electronic-data-capture/software)

## Links

- [View on SoftwareAdvice](https://www.softwareadvice.ie/software/560989/ACTide-eCRF)

## This page is available in the following languages

| Locale | URL |
| en | <https://www.softwareadvice.com/product/560989-ACTide-eCRF/> |
| en-AU | <https://www.softwareadvice.com.au/software/560989/ACTide-eCRF> |
| en-GB | <https://www.softwareadvice.co.uk/software/560989/ACTide-eCRF> |
| en-IE | <https://www.softwareadvice.ie/software/560989/ACTide-eCRF> |
| en-NZ | <https://www.softwareadvice.co.nz/software/560989/ACTide-eCRF> |

-----

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Customers can configure and manage studies independently, collaborate with the ACTide team, or outsource selected activities such as database design, validation, data management, and study support. This makes the platform suitable both for organizations with established internal clinical operations and for teams that require additional expertise or resources.\n\nThe system is designed for regulated clinical research environments and supports requirements and principles including ICH-GCP, GDPR, ISO Certifications, ALCOA+, CDISC/CDASH standards, and electronic record and signature controls. ACTide’s Validation Factory provides a structured approach to platform and release validation, helping customers reduce the effort required to maintain a controlled and inspection-ready environment.\n\nACTide helps study teams address common operational challenges such as fragmented systems, manual processes, inconsistent data, delayed query resolution, limited study visibility, and complex vendor coordination. By bringing multiple clinical capabilities into one ecosystem, the platform supports greater data consistency and more efficient collaboration among sponsors, CROs, sites, monitors, data managers, and patients.\n\nIts configuration tools allow authorized users to create and update studies without depending entirely on vendor development cycles. Features such as field-level source data verification, visit signatures, multilingual capabilities, role-based access, audit trails, data exports, dashboards, and configurable workflows help teams adapt the platform to different protocols and study designs.\n\nACTide Insight AI extends these capabilities by allowing authorized users to interact with clinical data through natural-language questions and generate real-time insights, dashboards, and exports. The objective is to make study information easier to access while keeping data governance, traceability, validation, and human oversight central to the process.\n\nACTide can support clinical trials involving medicinal products, medical devices, and veterinary research across different phases and geographical locations. The platform is particularly suited to organizations seeking a long-term technology partner, a flexible implementation approach, and an alternative to rigid, disconnected clinical systems.\n\nRather than offering software alone, ACTide combines technology, clinical data management expertise, validation services, and ongoing customer support. 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