Speed submission timelines and Improve data quality at Arena Clinical Data Management 2026

The Pinnacle 21 Enterprise platform is designed to transform and accelerate the clinical data lifecycle with precision and efficiency. Powered by our advanced Clinical Metadata Repository, it enables faster cycle times, from study setup to database lock – ultimately driving the rapid development of life-saving therapies.

Our cloud-based solution is recognized for its reliability and innovation – proudly adopted by the FDA, the PMDA, 24 out of the top 25 biopharmaceutical companies, and 12 of the top 15 leading global CROs.

By leveraging Pinnacle 21 Enterprise, organizations can build studies with unparalleled speed and accuracy, ensuring compliance and operational excellence.

Presentation

Tuesday, September 9 , 11:45am

標準化eCRFがもたらす価値 ― データ収集から申請まで

講師： Jen Manzi, Subject Matter Expert

Case report forms are the foundation of clinical data collection. They determine what data is captured, how it is captured, and how much confidence there can be in the result. Yet in many organizations, forms are still built in Excel, Word, or ad-hoc formats that rarely align with EDC requirements or with each other.

This session examines how that inconsistency can affect the clinical data lifecycle from study build through regulatory submission, and explores the role of high-quality CRF design, standards, reusable content, and technology in improving consistency, efficiency, and traceability. The session will also demonstrate how these concepts can be put into practice through CRF creation and EDC execution, supported by a real-world case study.

Watch this short video and see how to achieve submission ready conformance with Pinnacle 21

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