Meditrial Europe Ltd.
Meditrial is a Swiss-headquartered full-service Clinical Research Organization (CRO) focused on clinical trials, regulatory affairs, medical education and market access for the medical device, pharma and biotech industries.
Last updated September 29, 2026
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Overview
Meditrial Europe Ltd. is a Clinical Research Organization (CRO) headquartered in Zürich, Switzerland, with additional offices in Rome, Berlin and New York. Established in 2008, the company positions itself as a full-service partner for the medical device, pharmaceutical and biotechnology industries, with a particular emphasis on the medical device sector. Its services span clinical trial management, regulatory affairs, market access representation and medical education. Meditrial describes itself as a leading CRO dedicated to clinical trials, medical education, regulatory affairs and market access, combining medical expertise, execution discipline and an intuitive digital platform. The company states that it is focused on the needs of the medical device industry and serves innovative life sciences companies developing breakthrough devices that require a strategic path to first-in-man and pivotal clinical studies. It reports an outstanding record of 100% success in assisting clients with clinical investigation approvals. Operationally, Meditrial provides full clinical trial management in Europe, including site selection, study approval, site initiation, clinical data management, biostatistics and risk-based monitoring. It also offers market access services such as US Agent, EU Representative, UK Responsible Person, Swiss Representative, GDPR Representative and Data Protection Officer roles. Through its MasterTrial platform, it provides certified training, exclusive courses and live events on evolving regulations. Its proprietary cloud-based software solutions, including EDC and app solutions, are designed to give doctors and patients real-time access to online live data. The company manages projects across multiple therapeutic areas, including cardiac valve repair and replacement, structural heart interventions, coronary and peripheral interventions, cardiac ablation and pacing devices, neurology and neurovascular, ophthalmology, diagnostic devices and orthopedics. Meditrial is headquartered in Zürich and maintains offices in Rome, Berlin and New York.
History
Meditrial Europe Ltd. was established in 2008. From its headquarters in Zürich, Switzerland, the company grew into a full-service Clinical Research Organization (CRO) serving the medical device, pharmaceutical and biotechnology industries. It expanded its operational footprint with offices in Rome, Berlin and New York, enabling it to manage clinical trials across Europe and provide market access representation in multiple jurisdictions. Over the years, Meditrial developed a focus on the medical device sector, positioning itself as a partner for companies developing breakthrough devices that require strategic pathways to first-in-man and pivotal clinical studies. The company reports an outstanding record of 100% success in assisting clients with clinical investigation approvals. It has built proprietary cloud-based software solutions, including EDC and app solutions, to support clinical data management and patient engagement. Meditrial also operates MasterTrial, a certified training platform offering exclusive courses and live events on evolving regulations. Its market access services include acting as US Agent, EU Representative, UK Responsible Person, Swiss Representative, GDPR Representative and Data Protection Officer. The company manages projects across therapeutic areas such as cardiac valve repair and replacement, structural heart interventions, coronary and peripheral interventions, cardiac ablation and pacing devices, neurology and neurovascular, ophthalmology, diagnostic devices and orthopedics.
- 2008
Meditrial Europe Ltd. established.
Opened offices in Rome, Berlin and New York.
Launched MasterTrial certified training platform.
Products and positioning
A leading full-service CRO focused on the medical device industry, combining medical expertise, execution discipline and an intuitive digital platform to accelerate market access for life-changing therapies.
Clinical Trial Management
Full-service trial management including site selection, study approval, site initiation, clinical data management, biostatistics and risk-based monitoring.
Market Access Services
US Agent, EU Representative, UK Responsible Person, Swiss Representative, GDPR Representative and Data Protection Officer services.
MasterTrial
Certified training platform with exclusive courses and live events on evolving regulations.
EDC and App Solutions
Proprietary cloud-based software allowing doctors and patients real-time access to online live data.
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