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ClinCapture's Latest Updates: eTMF and Enhanced Audit Log Features

Las Vegas, March 18, 2025 — ClinCapture, a leading provider of clinical trial management solutions, has announced the launch of two innovative feature enhancements that promise to transform study documentation and audit processes for clinical research organizations across the globe.

Revolutionizing Document Management with eTMF Capabilities

The new electronic Trial Master File (eTMF) functionality offers a suite of powerful tools for managing study documentation efficiently. Key features of the eTMF include:

• - Safe Document Storage: Users can securely archive all study-related documents in a centralized digital repository, ensuring easy access while maintaining confidentiality.
• - Organized Study Folders: The ability to create dedicated folders for each study helps in organizing documents efficiently, making retrieval straightforward.
• - Site-Specific Document Storage: Enhances security by allowing storage specific to individual study sites with customized access.
• - Version Control: Facilitates tracking of document revisions over time, maintaining a historical record effortlessly.
• - Manage Permissions: Users can customize document access, ensuring sensitive information is shared only with authorized personnel.

Scott Weidley, CEO at ClinCapture, stated, “Our new eTMF capabilities provide researchers with a seamless and secure document management experience. By centralizing both study and site documentation and offering granular permission controls, we empower our users to manage their documents in ways that suit their unique requirements.”

Streamlining Audit Processes with Enhanced Subject Audit Log Export

In addition to improved document management, ClinCapture has unveiled the Enhanced Subject Audit Log Export feature. This new function provides:

• - Comprehensive Subject Exports: Users can now quickly generate detailed audit logs for every subject associated with a specific study site.
• - Key Insight Filtering: All relevant data can be neatly aggregated in one CSV file, allowing users to easily identify trends and insights.
• - Increased Efficiency: By eliminating the need to download logs individually for each subject, this feature significantly improves the review process.

Amanda McLean, VP of Sales and Customer Enablement, remarked, “The Enhanced Subject Audit Log Export feature is a game-changer for our users. It simplifies the audit process, enabling clinical research teams to focus more on analysis and decision-making rather than cumbersome administrative tasks.”

Key Benefits for Users

ClinCapture's enhancements yield several key benefits for users, including:

• - Centralized Documentation: Users can keep all study and site documents in one easily accessible location.
• - Customized Organization: The document management system can be tailored to meet the distinct needs of each study, enhancing usability.
• - Enhanced Permission Control: Maintains strict control over who can access documents, ensuring data security and compliance.
• - Time-Saving Exports: Generating comprehensive audit logs has never been quicker, leading to overall efficiency improvements.
• - Insightful Data Filtering: Users can easily spot trends and patterns across various study parameters, enhancing oversight and reporting capabilities.

ClinCapture’s unwavering commitment to innovation in clinical research is vividly showcased through these new feature releases aimed at supporting efficient study management and robust data analysis.

For more details about these exciting new features or to schedule a product demo, visit ClinCapture.com or reach out to their press team at press@clincapture.com.

About ClinCapture

ClinCapture is a leading provider of clinical trial management solutions, dedicated to empowering research teams with secure, innovative, and effective tools. With a focus on boosting productivity and ensuring compliance, ClinCapture is continuously setting the standard in clinical research technology.