
OUR EXPERTISE
STUDY DESIGN AND IMPLEMENTATION
-
Dedicated clinical trials clinic
-
Conduct of trials in-house, from patient recruitment, screening, randomization, follow-up, eCRF entry, AE and SAE assessment, preparation and attendance in audits, to drug registration.
-
Scientific advice design of phase 2,3, and 4 trials
PATIENT RECRUITMENT
-
Expansive network of patients with database of 20,000+ Chinese patients for rapid recruitment in Hong Kong
-
Validated methods of recruitment by electronic media
-
Community outreach activities with 100+ community organizations
QUALITY ASSURANCE
-
Dedicated QA and QC team
-
Real-time response to queries by investigators and coordinators.
REGULATORY AFFAIRS CONSULTATION
-
Our team advises on the most up-to-date regulatory and ethic requirements in China and Hong Kong to ensure that all trials are compliant with local legislation and regulations.
-
Strong experience with global regulatory authority audits including FDA (USA), CFDA (China) and EMEA (European Union) leading to trial drugs registered globally.