Increase the efficiency of your studies
by digitizing, automating and standardizing routine processes and with real-time reporting, automated alerts and risk-based monitoring, dashboards and overviews.
Reduce study-related costs
by significantly boosting the productivity of your staff through streamlined communication with clinics, registry databases and sales representatives.
Generate reliable & consistent data
that meet the highest scientific requirements and facilitate submission to authorities (notified bodies, FDA, etc.) and scientific publications.
Fulfill regulatory & data protection requirements
such as MDR, GDPR, ISO 13485, HIPAA, 21 CFR Part 11, 21 CFR Part 820, IEC 62304, BDSG and GCP reliably and hassle-free.
Gain trust & reputation
through a visible commitment to evidence-based medicine, increased transparency, and proven product performance and safety.