CMIC’s Vietnam office provides full operational services in the execution of clinical trials under the Pharmaceutical Value Creator (PVC) model. Our combination of industry experience and expertise across a broad spectrum of therapeutic areas and phases can help you accelerate clinical and commercial success to deliver better medicines, sooner.

Vietnam has a large pool of treatment-naive patients, but patients must often travel distances in order to access major cities with hospitals. CMIC ensures the selection of sites that have an accessible patient population.

Services

  • Regulatory consultation and dossier submission to health authorities (HA) and ethics committees (EC)
  • Clinical monitoring and site management
  • Full Biometrics support and Clinical Study Report (CSR) writing
  • Pharmacovigilance and medical monitoring
  • Quality assurance and quality compliance services
  • Project/Vendor Management

Facility Contact Information

Unit S. 22, 31st Floor, Saigon Trade Center, 37 Ton Duc Thang Street, Ben Nghe Ward, District 1, Ho Chi Minh City, Vietnam

Tel: +65 -6222-2655
Fax:+65-6222-2605

Business Inquires
Email: information@cmic.co.jp

Careers

Asia Clinical Trials

Regulatory Consulting

Pharmacovigilance

Quality Assurance