A powerful console to help you create the latest eCRF layout, inline checks and database structure or re-use archived ones for fast prototypes and finalized environments.
A flexible, role-based data capture system to safely collect study data in its compliant and validated database.
A web-based module to capture eDiaries and questionnaires data within the same database of the eCRF with the convenience of using your own device of choice.
A secure and practical access point for TMF study documentation, supporting all essential document processes and reducing TMF management timelines, costs and risks.
A robust set of tools to centrally verify study data with ease, from multiple points of view and even remotely.
Data Management Tools and Services
A revolutionary set of tools that allows data controls to be set and run at any time in the background rather than on the eCRF where Investigators need quick and simple forms.
A fully configurable reporting system that delivers an intuitive insight of how patient data evolve over time.
Project Management Tools
A new paradigm for data management that delivers hands-on ability to maintain tight and responsive control over the study data (e.g. charts, KPIs, etc).
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 flexible and affordable solution for the pharmaceutical industry. Optional modules, along with a flexible service model, allow you to tailor the solution to the real needs of your projects/studies, thereby lowering the TCO per study by minimizing system complexity.
EDC medical device clinical trials software must meet a variety of requirements related to connectivity, security, privacy, API integration, and specific interfaces to hardware. Medical device companies must be forward-looking and provide their data to post-market safety surveillance, compliant with regulatory authorities’ expectations.
ACTide complies with VICH GL9 (CGP) and is the perfect solution for your clinical animal health trials. Specific features have been created and configured to meet the particular 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 favorable price level, even for low budget or non-profit projects. Added to this is the ability to further split the TCO by outsourcing part of the study's CRF design process.
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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