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An ecosystem for eCRF, EDC, ePRO, compliance, and analytics, designed to deliver autonomy, speed, and security to sponsors, CROs, and research teams.
At its core is Insight AI, the module that brings artificial intelligence
into your clinical research.
No more slow reports or costly customizations:
Insight AI means full control of data, instant efficiency, and faster decisions.
With ACTide Ecosystem, the future of clinical trials is already here.
The ACTide ecosystem is designed to transform the way you conduct clinical trials, while making each user’s activities and tasks easier, faster, and more enjoyable.
The ACTide Designer, the ACTide eCRF are the core of the solution, allowing you to design, manage and execute your clinical study from scratch. From there, pick and choose from a range of fully integrated modules – each specially developed to simplify and boost a particular aspect of your trial.
The seamless integration of the ACTide modules allows you to move fluidly between the applications within the solution, and when combined they provide real value to your clinical trials.
ACTide ePRO
Pharma
Electronic Data Capture (EDC) for Pharmaceuticals.
Dynamically build and deploy Clinical Trials that leverage data from any source on our platform. Efficiently manage data for your trials and registries on the top-rated electronic data capture system.
Medical Devices
Navigate Medical Device with Ease.
No matter your level of expertise, ACTide eClinical ecosystem allows medical device to build a technology foundation that meets varying study and regulatory needs.
Animal Health
The first EDC For Animal Health.
ACTide Electronic Data Capture (EDC) system power companion and farm animal research for almost every major animal health company.
We work with veterinary clinics and production farms, across a variety of species, on studies and registries in all stages of the research process.
Non profit
One Clinical Trial Management System to power people, processes, and progress.
ACTide support Non Profit organizations to adapt, simplify, scale, and accelerate your Clinical Trials, from protocol design, to study startup, conduct, and close-out.
Electronic systems are increasingly used in clinical market. To comply with
regulations, these systems must undergo validation testing to ensure they are fit for purpose.
Healthcare facilities can rely on Nubilaria’s Validation as a Service (VaaS), a
computer system validation service specifically designed for the clinical setting.
Nubilaria’s VaaS offers an efficient process that allows healthcare facilities to comply
with validation regulations, streamline the validation process and focus on delivering
quality care to their patients.
We aim to consider our customers more as partners than simple buyers of our solutions and settle a flexible collaborative approach.
We give them the freedom to choose the level of involvement in the implementation of the projects and the workflow’s management.
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.
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