ACTide® eCRF

Unlock the potential of electronic Case Report Form (eCRF) in Modern Clinical Trials with Nubilaria ACTide®

ACTide® eCRF
Unlock the potential of electronic Case Report Form (eCRF) in Modern Clinical Trials with Nubilaria ACTide®.

In the ever-evolving landscape of clinical Trials, Electronic Case Report Forms (eCRFs) have emerged as indispensable tools, revolutionizing the way data is collected and managed. 

What are Electronic Case Report Forms?

Electronic Case Report Forms, or eCRFs, are digitalized versions of traditional paper-based case report forms used in clinical trials. The electronic forms streamline the data collection process, offering a more efficient and accurate alternative to the cumbersome paperwork of the past.

Since 2008 we have been developing our proprietary eCRF named Nubilaria ACTide®, the full state-of-the-art system.

actide software

The Advantages of the ACTide® eCRF

Time Efficiency

You can accelerate data collection and data entry, reducing the time required to complete clinical trials.

Data Accuracy

With built-in validation checks and real-time error alerts, we can guarantee the accuracy of your data, minimizing the risk of discrepancies.


The transition to ACTide® eliminates the need for paper, printing, and storage, resulting in significant cost savings.

Remote Accessibility

Researchers can access ACTide® from anywhere, facilitating collaboration and enabling remote monitoring.

The Benefits of the ACTide® eCRF

User-Friendly Interface

ACTide® has an intuitive interface accessible to all the dedicated profiles with varying levels of technical expertise.

Data Security

Advanced encryption and secure data storage protocols safeguard sensitive information, ensuring compliance with regulatory standards.


ACTide® can be tailored to meet the unique requirements of your studies, providing the flexibility you need in data collection.

The Key Features of the ACTide® eCRF:

  • Standard and customized user profiles.
  • Alerts and notifications system.
  • Online audit trails.
  • Monitoring & SDV tools.
  • Automatic clarifications.
  • Real-time data exports.
  • Unlimited users and sites.
  • Document sharing within study/site crew.
  • Pre-loaded laboratory ranges.

Everything in the ACTide® eCRF is validated, from the core of the software to dedicated single project and integration, to other software or devices. ACTide® eCRF is compliant with  user requirements and the applicable regulations and guidelines (i.e.: ICH GCP, 21 CFR Part 11, GMP Annex 11, ISO 14155 – Medical Device, and GDPR).

As the digital era continues to reshape clinical research,  the ACTide® eCRF is a testimony to progress. We can adopt ACTide® eCRF not only to enhance efficiency and accuracy but also to pave the way for more innovative and collaborative approaches to scientific inquiry. 

Embrace the future of data collection with ACTide® eCRF, and elevate the impact of your research endeavors.

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