Clario's Clinical Adjudication solution is a comprehensive platform designed to manage Clinical Event Committees (CECs) in clinical trials efficiently and effectively. It combines experienced project management, deep clinical expertise, and an advanced web-based platform to streamline the entire adjudication process. The solution offers rapid study initiation, expert guidance on charter design, and a centralized repository for all trial-related documents and data. It ensures compliance with regulatory requirements, enhances data quality through AI-powered de-identification, and provides seamless integration with third-party applications. With a global network of medical experts covering various therapeutic areas, Clario offers specialized knowledge when needed. The platform also provides full data transparency with visual performance metrics and round-the-clock live support, aiming to improve the efficiency, accuracy, and quality of clinical trial adjudication processes.

Key Features

Experienced Project Management Clario's team of program and project managers brings over 100 years of cumulative experience in clinical trial adjudication.

• Rapid launch of new studies or transition of existing data
• Full management of CEC meeting coordination
• Support for global trials with localized language support and translated materials

Clinical Domain Expertise A vast global network of medical experts specializing in specific clinical trial endpoint therapeutic areas.

• Expert guidance on charter design
• Access to key opinion leaders across various therapeutic areas
• Insights throughout the trial with full data transparency

Comprehensive Web-based Platform A centralized online repository for managing the clinical trial adjudication process.

• 100% de-identification of all source documents using AI technology
• Compliance with 21 CFR Part 11 and EU GDPR requirements
• Automatic routing and de-identification to reduce manual errors
• Integration with 3rd-party applications like EDC and safety systems
• 24/7/365 live support via chat, phone, or email

Benefits

Enhanced Data Quality and Security Improves the overall quality and security of clinical trial data.

• AI-powered de-identification ensures patient privacy
• Compliance with regulatory requirements
• Reduced manual errors through automation

Streamlined Adjudication Process Simplifies and accelerates the clinical trial adjudication workflow.

• Centralized repository for all trial-related documents and data
• Efficient coordination of CEC meetings
• Rapid study initiation and seamless transitions

Global Reach and Expertise Provides access to a wide range of clinical expertise and supports global trials.

• Specialized knowledge in various therapeutic areas
• Support for multi-country trials with localized resources
• Access to key opinion leaders and veteran adjudication specialists