Increase the efficiency of your trials
by digitizing, automating and standardizing routine processes and with real-time reporting, automated alerts and risk-based monitoring.
Keep track of all trial-relevant data
with dashboards and overviews, reports on missing data and well-formatted, easy-to-understand biostatistical reports.
Plan trials, quickly & easily
via drag & drop and self-defined criteria for automated patient preselection based on freely defined medical history questionnaires and image analysis.
Reduce trial-related costs
by significantly boosting the productivity of your staff through streamlined communication with clinics and sponsors with the help of our web-based, installation- and maintenance-free system.
Delegate regulatory & data protection requirements
such as HIPAA, 21 CFR Part 11, 21 CFR Part 820, IEC 62304, ISO 13485, GDPR and BDSG.