The complete eClinical solution provided by Nubilaria

view more

EUROLogin 2020

Initiative co-financed by the European Commission through the CEF Telecom programme, managed by HaDEA

view more


Although ACTide® is used by all types of customers and industries -whether they are Pharmaceutical or Medical Device companies, research institutions, non-profit organizations, or hospitals-, it is CROs that are historically the designated target audience for our platform. ACTide® is fully featured with the Sponsors’ most requested functionalities; it also comes with an encompassed flexibility in terms of configuration, usage, and pricing that make it the perfect solution for CROs.
ACTide®'s clinical services are the perfect companion to your projects based on our platform and are declined with the same level of flexibility. Our data management team is engaged with your project from the very beginning until the study decommissioning to support your team throughout the study lifecycle.



ACTide® is the right, flexible and affordable solution for the pharmaceutical industry. The optional modules available in the platform, together with its flexible service model, allow you to tailor the solution to the real needs of your projects/studies, and therefore lowering the TCO per study by minimizing the system complexity.


EDC software for medical device clinical trials must fit with a variety of requirements involving connectivity, security, privacy, API integration and specific interfaces to hardware. Medical device companies need to be forward-looking, providing their data to post-market safety surveillance, compliant with regulatory authorities' expectations.


Being XXX compliant, ACTide® is the perfect solution for your Animal health clinical Trials. Specific features have been created and configured to answer the peculiar needs of Data Capture in Animal Health scenarios.


The flexible service model and the extreme granularity in the configuration of the CRF, allow a very convenient level of pricing even for low budgets projects or for non-profit projects. To this is also added the possibility of further breaking down the TCO by insourcing part of the design process of the study's CRF.


eCRF Self-Configuration

ACTide® flexible workflow gives your project-managers unlimited freedom to design and configure your eCRF. It helps create validation rules, manage users and sites. You can define and set normal ranges for laboratory data, preview your draft at any time to have a working environment to show to your customers.

Intermediate Tactical Choices

Rely on the ACTide® Team for complex or critical tasks and use your staff for the rest. You decide the balance between internal and external effort to match your budget requirements and your production pipeline.

Full Service by Nubilaria

Fully delegate to the experienced ACTide® Team staff the task of building and validating your eCRF and see the magic happen. Focus your team on your core duties and tasks and let the ACTide® Team to complete your eCRF fully compliant with project requirements.


Learn how our 10 years of experience is helping our clients accelerate their clinical trials by ensuring data quality.

The Neurological Institute Carlo Besta, in conjunction with the Italian Ministry of Health, has developed and validated a protocol for the early diagnosis of Alzheimer. Such protocol includes a research phase on “biological and generic markers”, diagnosis, cognitive-behavioural tests and guidelines...

Read more

News & events

All / Events / News

SCOPE 2021 Virtual

SCOPE - Summit for Clinical Ops Executives

Read more
EUROLogin 2020

EUROLogin 2020

Read more
ACTide against COVID-19

DECEIVER trial for COVID-19 related ARDS intensive care

Read more


Want more information about our solutions?
Contact us today.