secuTrial

secuTrial is a web-based software solution designed for the management of clinical trials, patient registries, and other medical research studies. It caters to organizations of all sizes, from small research institutions to large pharmaceutical companies. Clinical researchers, medical professionals, pharmaceutical companies, contract research organizations (CROs), and academic institutions are among the users of secuTrial.

Key Features

Randomization Algorithms: secuTrial offers a variety of algorithms for randomization, including single block randomization, static unstratified multi block randomization, static stratified block randomization, and simple randomization. These algorithms support different randomization groups and blind settings, while taking into account stratification factors based on patient characteristics.

Import Function for Catalogues: secuTrial provides a convenient import function for catalogues, allowing users to easily transfer data from external sources into the system. This feature eliminates the need for manual data entry, saving time and reducing errors. Users can import catalogues such as SPSS exports, enabling seamless integration of data from different sources.

Workflows for Monitoring: secuTrial offers specialized workflows for monitoring clinical trials and studies. These workflows streamline the monitoring process, ensuring systematic and efficient completion of all necessary steps and tasks. By enhancing data quality and compliance with regulatory requirements, the monitoring workflows contribute to the success of studies.

Multiple Customer Management: secuTrial supports the management of multiple customers, enabling users to efficiently handle different projects and studies for various clients. This feature allows for easy organization and tracking of data for each customer, ensuring data security and confidentiality. Users can seamlessly switch between projects and maintain separate data sets for each customer.

CDISC Export 1.2.1: secuTrial supports CDISC export 1.2.1, facilitating the exchange of clinical trial data with other systems and stakeholders. This feature ensures compatibility and interoperability with industry-standard data formats, enabling seamless data sharing and collaboration. CDISC export enhances data standardization and simplifies data integration processes.