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	Clinical trial design and organization: familiar with clinical trial of Oncology, Immunology, Nuclear Medicine, Neurology，Pharmacy，Botanic Medicine, IVD and Medical device.

	Medical writing：Clinical protocol, investigator’s brochure (IB), clinical study report (CSR) and common technique document （CTD） for IND.

	Regulatory application ：familiar with ICH, GCP, EMA and US-FDA guideline.

	Clinical and research consultation：provide professional advice for drug development, assist the company to cross the academic gap. 

	Business Development: Assist the business exploration in Asia pacific region.

	Biomedicine and academic research: with more than 10 years, 

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