Solutions for
CROs &
Research Centers
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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.

Your benefits

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.

Regulatory requirements

UNITY centralizes and automates numerous routine tasks related to the planning and monitoring of clinical trials. As a result, data quality can be increased and studies can be conducted in an efficient, transparent and cost-effective manner.