Our Vision

Our vision is to deliver clinical trials with greater clarity, efficiency and confidence through trusted digital platforms. By strengthening how clinical evidence is generated, the Medigen Suite™ contributes to a healthier world through better research, informed decision-making, and more effective medical innovation.

Connected Healthcare Systems

As a digital health platform, we envision a future in which digital intelligence is seamlessly embedded across healthcare systems, enabling care that is more connected, data-driven, and resilient at scale. The Medigen Suite™ empowers sponsors, CROs and research teams to generate actionable insights, support both personalized and population-level care, consistent execution, and integrated oversight across studies, regions and trial models.

Collaboration & Integration

Connected teams and integrated digital systems drive better clinical trials. By unifying sites, sponsors, and study teams through shared eClinical workflows, we support efficient execution, clear oversight and consistent trial delivery.

Integrity & Trust

High-quality clinical research relies on transparency and accountability. We uphold trust through compliance ready systems, auditable processes, and strong data governance aligned with global regulatory standards.

Data-Driven Excellence

Reliable decisions depend on accurate clinical data. We promote high-quality data to support real-time oversight, risk-based trial management and actionable insights across the study lifecycle.

Patient Centricity

Patients remain central to every trial. We design patient-friendly digital experiences that respect safety, privacy and time, supporting participation through eConsent, ePRO and decentralized trial capabilities.

We believe eClinical platforms should adapt to clinical workflows — not the other way around. Our focus is on building flexible, secure and interoperable solutions that support the full clinical trial lifecycle while meeting global compliance expectations.

Monica Tocchi, MD. PhD
Founder and CEO at Meditrial CRO and Medigen Suite

Compliance at the Core

Medigen is developed by Meditrial, an organization certified to ISO 9001, ISO/IEC 27001, ISO/IEC 27701, and ISO 13485. It is designed to support global regulatory and data protection requirements, including FDA 21 CFR Part 11, GDPR, HIPAA, CDISC, and ICH-GCP. This commitment to quality management, information security, and privacy underpins the Medigen Suite, supporting secure, reliable, and compliant eClinical platforms for clinical trial management.