Top 5 Reasons to Choose Clinion’s AI-Enabled eClinical Platform for your next trial

Choosing the right eClinical platform vendor is the cornerstone of successful trials. An inadequate choice can lead to a cascade of challenges, from data inaccuracies to operational inefficiencies.

In this complex landscape, Clinion isn’t just a platform — it’s a seasoned guide adeptly navigating clinical trials with transparency, precision, and an innate understanding of the challenges.

Now, let’s break down the core reasons why Clinion is the linchpin for your clinical trial success.

Clinion’s platform is designed with you in mind. From trial inception to completion, our eClinical platform prioritizes user needs, ensuring a seamless and user-friendly journey. The system is built to be accessible and relevant to the specific needs of different users.

• We prioritize user-friendly interactions to enhance efficiency and reduce the learning curve for all stakeholders.
• By providing role-specific dashboards and features like global libraries, we ensure that each user maximizes trial efficiencies without unnecessary complexities.
• Clinion strives for simplicity and speed. By actively incorporating user feedback, we ensure continual refinement for optimal efficiency.

Supporting the diverse landscape of clinical trials requires a platform that can adapt and evolve. Clinion empowers researchers to handle the complexities of modern clinical trials with ease. Whether it’s a simple trial or a highly complex study ( DCT, hybrid, or any therapeutic area) our platform adapts seamlessly, providing robust functionality for every type of clinical research.

• Clinion’s scalability allows for the smooth integration of modules, adapting effortlessly to the intricacies of your research, be it a single-site trial or a complex multi-arm study.
• Our systems are put to the test in countless clinical trials, ensuring your data and processes remain resilient and dependable.
• The safety and integrity of data are guaranteed, with compliance with regulatory standards such as ISO 9001, ISO 27001, GDPR, and ICH GCP.

Clinion stands as a unified solution catering to the diverse needs of clinical trials. This holistic approach ensures a seamless and integrated experience, addressing every aspect of trial management with a unified strategy.

• The platform is integrated ensuring cohesion across every phase, eliminating the hassle of juggling multiple systems.
• Minimizes data silos, and reduces manual work, by creating a unified hub for all your trial needs.
• Access central lab data, EDC, and data from external sources, including ePRO, within a single system in the fastest and most reliable manner.

Clinion propels clinical trials into the future with the integration of Artificial Intelligence (AI). This forward-thinking approach enhances efficiency, accuracy, and overall trial success by harnessing the power of cutting-edge AI technology.

• AI medical coding swiftly assigns accurate codes based on provided terms, reducing coding time by 70%-80% compared to interactive coding.
• CSR Automation helps you generate 70% of the report allowing for faster submissions.
• eProtocol reduces protocol design times and disruptions by providing optimal protocols from the knowledge base, minimizing amendments.
• Automated Source Data Verification (SDV), which systematically checks and validates trial data, guaranteeing accuracy and efficiency in a blink.

Clinion doesn’t just streamline clinical trials; it significantly reduces the cost of ownership. Our platform is engineered to optimize resource utilization, enhance operational efficiency, and ultimately minimize the financial footprint of managing clinical trials.

• We offer a flat per study per month pricing model that facilitates transparency and fairness.
• Clinion offers AI capabilities at the cost of traditional systems giving unparalleled value for your investment.
• Enhance your system with value-added features like data loader and AI medical coding at no extra cost.

In conclusion, clinion emerges as a solution adept at addressing the clinical data challenges faced by clinical trial professionals. By enhancing the collaboration and management of sensitive data among sites, contract research organizations, sponsors, and trial participants, clinion proves to be a valuable ally in ensuring a smooth and streamlined experience throughout the trial process.

The best way to truly grasp the Clinion advantage is to experience it firsthand