Study Management offers the following benefits:
Automizes the entire administrative process regarding the request, approval, and execution of clinical studies.
The application is fully adaptable to the processes
The process is adjustable per type of study
Submitting and managing the research protocol in just one environment
Send CTA letters with one press on the button
Adjustable notifications targeted on role distribution
Immediately develop a Statement Suitability Clinical Trial Site (SSCTS)
Document management in one place
Real-time dashboard with management information
Complies with the 'Good Clinical Practice' principlesAudit Trail, Role Based Access Management, built-in notifications, ISO27001 & NEN7510 certified.
Can be linked with MERC Management from Research Manager