Solutions for the
Medical Device
& Pharmaceutical
Industry
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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.

Your benefits

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.

Regulatory requirements

UNITY centralizes and automates numerous routine tasks related to the management of clinical trials and postmarket (PMCF) studies. As a result, studies can be conducted in an efficient, transparent and cost-effective manner for faster time to market.