studioMED+

This refers to the core function of storing and managing all study-related data in a central, electronic format.

This feature allows users to create records for patients participating in studies, search for specific patients, and assign them to particular studies.

studioMED+ uses a central database to store all information.

The software is installed on a server within the organization's intranet, making it accessible to authorized users within the network.

This expands on the core data management by distinguishing between "master data" (information that is generally consistent across studies, like patient demographics) and "study-specific data" (information that is unique to a particular study, like study visit details or treatment information).

This feature allows for the secure storage and management of study-related documents (e.g., protocols, consent forms, investigator brochures). "Rights management" ensures that only authorized users can access, view, download, or modify specific documents.

The patient database stores information about study participants. "Encrypted" means the data is protected from unauthorized access. "Anonymous storage option" likely refers to features that allow for de-identification of patient data to protect privacy while still allowing for data analysis.

This feature enables the creation of visit schedules for patients participating in a study. The system can automatically generate appointments and send reminders to both patients and study staff.

This allows study teams to define tasks related to the study, assign them to specific individuals, and track their progress. This helps to organize study activities and ensure that tasks are completed on time.

This feature allows for tracking study-related expenses and allocating them to specific cost centers.

This feature provides a structured workflow for completing eCRFs, monitoring data entry, and evaluating the collected data. It likely includes features for data validation, query management, and electronic signatures.

This allows external investigators at different study sites to access and complete eCRFs for their patients. The system likely includes features for managing user access and permissions.