Medical software studyDESIGNER

analysisdata analysisdata management

studyDESIGNER simplifies GLP and non-GLP studies by managing data acquisition, data analysis, and reporting steps during toxicology and safety pharmacology studies. studyDESIGNER’s modular platform builds and organizes the study with fully integrated data management, workflow guidance, and automation at each stage of the experimental process. Automated post-processing capabilities shorten time to reporting. Built-in audit-trail and electronic signature capabilities ensure data integrity and accountability. Automated FOCUS ON WHAT’S IMPORTANT Users are guided in a stepwise manner through the various stages of the study – from study creation and study start through completion as well as archiving. User level access provides granular control for system admins and shows users only what they are able to use and configure. This reduces complexity for the users that really need to focus on the animals and not the software. The system is easily configured and designed for either long or short recordings from a few minutes to to multiple days. During recording sessions studyDESIGNER automatically drives our embedded IOX2 (data acquisition) and ecgAUTO (pattern recognition post-processing) applications to record and analyze data and send calculated parameters to its database. Defines the study: sessions, phase, subjects details, pre-test and treatment groups, experimental protocol, data collection and analysis settings. Guides users through data collection: acquires data on subjects planned for current sessions. Organizes data analysis: automatically on all recordings or according to subject or phase, reviews subject or global results.