Since the establishment of the Site Management Organization (SMO) business in 1999, EP-Link has acted as a bridge between the pharmaceutical companies that sponsor clinical trials and the medical institutions that conduct the trials, supporting the conduct of clinical trials at medical institutions. EP-Link is committed to responding flexibly to changes in the clinical trial environment, providing optimal solutions to customer needs, and further improving the clinical trial environment.
EP-Link contracts with medical institutions (clinical trial sites) to support clinical trial operations at medical institutions so that they can properly conduct clinical trials in accordance with GCP.
EP-Link supports the work of doctors, nurses, and secretariats involved in clinical trials, reducing the burden and improving the quality and speed.
More than6,000
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Approximately7,000
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Comprehensive Capacities
Management and Promotion
of Enrollment
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Management System
Quality Cross-organizational
Management System
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Management System
EP-Link has a large number of CRCs who can play an active role in therapeutic areas that require a high level of expertise, such as oncology, and support high-quality clinical trial work.
SDM leverages its experience as a Clinical Research Associate (CRA) to support data-related operations and help improve data quality in clinical trials.
With a high level of expertise and advanced skills as a clinical trial secretariat, SMAs support the arrangement of clinical trial implementation systems to meet various needs.
Rater Service EP-Link has a large number of assessment psychologists with clinical trial expertise who administer the rating scales required for CNS clinical trials.