Singapore Office

Established in 2006, CMIC Singapore serves as a regional hub, delivering comprehensive clinical trial operations through our Pharmaceutical Health Value Creator (PHVC) model.

With nearly two decades of experience managing both local and global projects across Southeast Asia, we possess an intricate understanding of the regional biopharmaceutical landscape. Our deep therapeutic expertise allows us to accelerate your path to commercial success.

Despite Singapore’s high trial density, our strategic site selection process identifies high-performing centers with sustainable patient access, ensuring your study stays on track in this sophisticated healthcare market.

Services

Regulatory & Ethics: Expert consultation, strategic dossier preparation, and seamless submission to Health Authorities (HA) and Ethics Committees (EC)
Clinical Operations: End-to-end clinical monitoring and comprehensive site management to ensure data integrity
Medical & Safety Oversight: Proactive pharmacovigilance and dedicated medical monitoring to ensure patient safety
Quality & Compliance: Comprehensive quality assurance (QA) and regulatory compliance services to mitigate risk
Strategic Management: Centralized project and vendor management for streamlined trial execution