Zelta

Zelta is a cutting-edge electronic data capture (EDC) system designed to streamline clinical trial data management. It offers a robust platform for capturing, managing, and analyzing data, ensuring that clinical trials are conducted efficiently and securely. Zelta's capabilities include protocol review, case report form (CRF) design, and database management, all of which are aligned with industry standards such as CDISC.

One of the key benefits of using Zelta is its ability to support complex clinical trial designs while maintaining compliance with regulatory requirements. It provides advanced data review and validation processes, ensuring that data is accurate and reliable. Additionally, Zelta facilitates seamless integration with other systems, such as electronic patient-reported outcomes (ePRO) and randomization and trial supply management (RTSM), making it a versatile tool for managing diverse clinical trial needs.

By leveraging Zelta, researchers and clinical trial teams can enhance their data management workflows, improve data quality, and accelerate the decision-making process. Its features are designed to support efficient clinical development, from study design to regulatory submission, making it an essential tool for organizations involved in clinical research.