Since 2019, CMIC Vietnam provides comprehensive clinical trial operations driven by our Pharmaceutical Value Creator (PVC) model. By merging deep industry experience with multi-phase therapeutic expertise, we help sponsors accelerate clinical development and bring life-changing medicines to market faster.

While Vietnam offers a vast population of treatment-naive patients, geographical distance to urban medical centers can present logistical challenges. CMIC overcomes this by strategically selecting high-performing sites that ensure both patient accessibility and study retention.

Services

  • Regulatory & Ethics: Strategic consultation and comprehensive dossier management for Health Authority (HA) and Ethics Committee (EC) submissions
  • Clinical Operations: High-standard clinical monitoring and proactive investigator site management
  • Medical & Safety Oversight: Integrated pharmacovigilance and dedicated medical monitoring
  • Quality & Compliance: Specialized quality assurance (QA) and regulatory compliance oversight
  • Project Leadership: Integrated project and vendor management to optimize study timelines and deliverables

Facility Contact Information

Room S19073, 19th floor, 3A – 3B Ton Duc Thang Street, Sai Gon ward, Ho Chi Minh city, Vietnam

Tel: +65 6222 2655

Business Inquires
Email: information@cmic.co.jp

Asia Clinical Trials

Asia Clinical Trials

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Regulatory Consulting

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Pharmacovigilance

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Quality Assurance