ACTide electronic Trial Master File (eTMF) supports studies of any scale and it is backed by a complete cloud-based document management system capable to manage study document workflows. Real-time collaboration between Sponsors and CROs is now the new standard.view product
ACTide eCRF is a configurable role-based permission system. It provides your study team and site Investigators with all the required tools and services to succeed in their daily tasks with the freedom of a Software as a Service.view product
With ACTide ePRO you can capture diaries and questionnaires data directly from your personal mobile device into the safety of an online database.view product
ACTide RTSM is a comprehensive tool to manage Randomizations and Clinical Trial Supplies.view product
ACTide sourceBOX provides Study Coordinators with a secure place where to redact and upload documents. It also serves CRAs providing them with a remote review and upload of their own monitoring reports.view product
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.
Learn how our 10 years of experience is helping our clients accelerate their clinical trials by ensuring data quality.
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