Top 4 Research Areas
Early Phase Studies
Over 20 years of experience
Over 170 early phase studies
Accredited by the National Medical Products Administration (NMPA) of China
Healthy Volunteer Database
Highlights of Clinical Trial Capacities
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Clinical Trial Personnel
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Clinical Trials Conducted
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Investigator with > 5 years experience
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M
Population Base
Starting Clinical Trial With Us
IRB Approval
6-8 weeks
Regulatory Approval
2-4 weeks
CTA Vetting & Approval
Less than 4 weeks
ABOUT CRMO
Clinical Research Management Office (CRMO) is a joint office established by The Chinese University of Hong Kong (CUHK) and the New Territories East Cluster (NTEC) of Hospital Authority (HA). CRMO provides comprehensive solutions for clinical trials conducting at the Prince of Wales Hospital (PWH) and other 6 hospitals/ 10 general out-patient clinics in the Cluster.
LOOKING FOR PARTNERSHIP?
Conduct your trial in a cost-effective and timely manner, contact us today!