CLINICAL RESEARCH MANAGEMENT OFFICE (CRMO)

Your Clinical Trial Partner in Hong Kong

Our Facilities

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CUHK/NTEC

A collaborative research network comprises of 6 hospitals and a teaching hospital of the Chinese University of Hong Kong (CUHK).

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Clinical Research Management Office

The Joint CUHK-NTEC Clinical Research Management Office (CRMO) aims to enhance the quality standards, efficiency and compliance of clinical trials through our comprehensive and tailor-made services. The CRMO also connects sponsors with suitable investigators, and facilitate various clinical research processes in the hospitals. 

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Phase 1 Clinical Trial Centre

World-class Clinical Trial Centre provides the top services

  • NMPA accredited Phase 1 unit
  • Dedicated research facility with access to Intensive Care Unit
  • Over 20 years of early phase research experience
  • Over 140 studies completed
  • Fully functional PK/PD Laboratory
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NATA and RCPA accredited clinical laboratories

The purpose-built laboratories are accredited by the National Testing Authority of Australia (NATA) and the Royal College of Pathologists of Australasia (RCPA) and provide on-site clinical sample analysis.

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CU-Med Biobank

CU-Med Biobank has been established for the standardized and systematic collection, storage and application of patient biological samples with standard operating procedures and quality manuals. This standardized CU-Med Biobank is a pivotal bridge to improve the translation of basic research into clinical applications.

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Clinical Research Pharmacy

The Clinical Research Pharmacy (CRP) provides central coordination and secure IMP management in compliance with ICH-GCP & regulatory requirements.