Clinical Research
HRI* (HEISU RESEARCH INSTITUTE CRO) services include regulatory affairs, clinical trial planning, site selection and initiation, recruitment support, clinical monitoring, data management, trial logistics, biostatistics, medical writing, and project management.
HRI CRO will also coordinate, executes, and manage the lifecycle of the clinical trials, safely and efficiently. Serving as the main contact between the sponsor and other stakeholders throughout the trial, the CRO communicates with ethics and compliance committees, regulatory personnel, vendors, physicians, and research coordinators.