Clinical trials play a pivotal role in bringing new drugs and medical devices to market, but they often come with challenges like high costs, time constraints, and lack of financial control. At Clinion, we understand these concerns, which is why we've developed a pricing model that sets us apart from the competition, empowering you to achieve unparalleled efficiency and success in your clinical trials.
Transparent and Flexible Pricing
Clinion's pricing structure is designed to empower you with complete financial control throughout your trial. We believe in transparency and fairness, which is why we offer a flat per study per month pricing model that includes cloud hosting, licensing and support. Say goodbye to hidden fees and unexpected expenses, and confidently plan your budget with Clinion.
Unlike traditional pricing models that depend on CRF pages, data points, users, or sites, Clinion's pricing is not based on these variables. This makes trial setup and management easier, regardless of complexity or size.
Mid-Study Changes without Extra Charges
We understand that mid-study/post-production changes are often necessary due to evolving protocols or design optimizations. Unlike some eClinical software vendors, Clinion empowers you to initiate changes on your own without the need of technical assistance or contacting support. Whether it's modifying forms, pages, or other study components, Clinion provides unmatched flexibility, enabling you to adapt seamlessly as your trial progresses.
Our customer support has received an impressive rating of 4.7/5 in multiple CSAT surveys, demonstrating their utmost satisfaction with our services.
Free Trial Access
At Clinion, we believe in empowering our users to take control of their studies with minimal dependencies.That's why we provide free access to our training/trial environment, enabling you to build and experiment with your studies independently and at your own pace. This reduces your training time and costs significantly, freeing up resources for other critical aspects of your trial. With Clinion, you're not just a customer but a valued partner, and we're committed to supporting your journey towards greater independence and efficiency.
Clinion delivers unparalleled value by offering AI-enabled features at the cost of traditional EDC systems. Our cutting-edge technology harnesses the power of AI and automation, delivering remarkable time savings throughout the trial process. Experience a significant 30-40% reduction in trial durations, leading to enhanced efficiency and streamlined operations. With Clinion, you can unlock faster, more accurate data collection and analysis, empowering you to make data-driven decisions with confidence. By embracing our AI-driven approach, you'll achieve impressive cost efficiencies without compromising on quality, setting new standards for excellence in clinical trials.
Special Pricing for Specific Trials
Clinion offers special pricing for Investigators Initiated, Research, and Registry Trials through its Clinion Lite offering. This makes the platform more accessible to trials with budget constraints. Clinion Lite provides the required features, but with reduced costs to make it more accessible to these types of trials.
Maximize Flexibility and Control in Clinical Trials
Global Library for Easy Study Setup
eCRF configuration and edit check configuration pose additional challenges in clinical trial management. Setting up eCRFs and edit checks requires trained resources, coding knowledge, and time. Clinion overcomes these challenges by its Global Library feature. This feature allows users to copy the eCRFs for an entire study or simply copy individual forms or pages from the library. Users can then modify them as per protocol requirements.All of this is possible by the regular data management team and does not require any coding expertise.
User-Friendly Drag-and-Drop Interface
The platform also provides a user-friendly drag-and-drop interface,ensuring that new and complex forms creation is a smooth and seamless process.
Versioning and Batch Edit Checks
The system's Versioning and Batch Edit checks features enable study configuration teams to make changes on their own and apply these changes to all subjects across the study or only to the subjects who would subsequently be enrolled. This not only reduces the cost of managing clinical trials but also increases the flexibility and agility of the trial.