About
Consultant in the Life Sciences & Healthcare Practice Group at Global Law Office with over 20 years' experience in pharmaceutical and medical device regulatory law in China and the U.S., advising on product licensing and collaboration, clinical trials, product registration, manufacturing, sales and marketing, pharmacovigilance, and pricing and reimbursement. Has provided pro bono assistance to the China NMPA and academic organizations on aligning China’s regulatory framework with international practices.
Practice areas
Life Sciences & HealthcarePharmaceuticalsMedical DevicesRegulatoryHealthcare Compliance
Office
Expertise
Pharmaceutical regulatory lawMedical device regulatory lawClinical trialsProduct registrationProduct licensing and collaborationsManufacturing and quality compliancePharmacovigilancePricing and reimbursement
Education
- University of Nebraska College of Law, J.D.
- Peking University, LL.B.
Languages
ChineseEnglish