

Medigen Suite offers a premier collection of intuitive clinical research solutions designed to streamline complex clinical trials. Their products include Electronic Data Capture, Clinical Trial Management Systems, and ePRO/eCOA applications, catering to various trial phases and sizes. The company targets organizations involved in clinical research, providing accessible and reliable cloud-based tools to enhance trial efficiency. With a focus on transforming the research experience, Medigen Suite aims to support clients in obtaining accurate results and improving data management.

Catchtrial® EDC+ is a next-generation clinical trial platform combining data capture, imaging, safety workflows, and AI-driven analytics in one integrated, secure environment. It enables real-time oversight, faster decision-making, and the delivery of high-quality, approval-ready data across global studies. Catchtrial® EDC+ serves as an intelligent clinical trial governance environment, where investigators, core labs, safety adjudication teams, monitors, and statisticians collaborate around real-time data — accelerating the delivery of reliable clinical outcomes.

Medigen® CTMS+ centralizes planning, monitoring, document management, product oversight and finances to streamline trials, reduce costs, and deliver faster, smarter results.

Catchtrial ePRO/eCOA is a patient-friendly electronic Patient-Reported Outcomes and Clinical Outcome Assessment platform. It delivers real-time symptom diaries, quality-of-life data, and validated instruments directly from patients on any device. Built for sponsors, CROs, biotech, pharmaceutical, and medical device organizations, the platform improves patient engagement, protocol compliance, and data quality while supporting GDPR, HIPAA, ICH-GCP, and 21 CFR Part 11 requirements.

Catchtrial® eConsent enables participants to review and sign informed consent from anywhere using telemedicine-inspired technology. Compatible with Android and iOS, it removes the need for on-site visits and provides a seamless, mobile-first experience for patients.

Mastertrial LMS+ is a validated Learning Management System designed for clinical trials. It delivers scalable, protocol-specific eLearning, investigator trainings with the certification to accelerate site activation and ensure GCP compliance.
Meditrial Europe is a clinical research organization specializing in providing comprehensive services for clinical trials, particularly in the pharmaceutical and biotechnology sectors. The company offers a range of solutions including project management, regulatory consulting, and data management, aimed at facilitating the efficient execution of clinical studies. With a focus on quality and compliance, Meditrial Europe supports clients in navigating the complexities of clinical development across various therapeutic areas.