ClinViet is a full service Contract Research Organization (CRO) whose management and clinical research personnel have a collective 30+ years of experience in the pharmaceutical, biotech, and medical device industry. We offer ICH-GCP compliant clinical trial services in our facilities in both the United States and Vietnam.

We bring clinical trial experience and expertise to Phase I-IV trials throughout a broad spectrum of therapeutic research areas, primarily focused on oncological, cardiovascular, and infectious disease research studies. We provide services to pharmaceutical and biotechnology companies, ensuring superior quality data, patient safety, and complete adherence to ICH-GCP standards of clinical research.

We start by conducting feasibility studies and continue on through study planning to regulatory submissions, site evaluation & selection, site monitoring, project management, medical monitoring, pharmacovigilance and quality assurance to provide the highest level of service.

ClinViet has an extensive network of sites in Vietnam, as well as facilities in the US. We have thorough knowledge of the Vietnamese regulatory process and close relationships with investigators and hospitals throughout Vietnam. We welcome individual doctors who wish to conduct clinical research, and we would be delighted to offer individuals interested in conducting clinical research trials in Vietnam the benefits of our services.