Jie LI
Principal advisor
About
Over 30 years of regulatory affairs experience in China
China
Beijing
Pharmaceuticals
Regulatory Affairs, Regulatory Submissions, Pharmacovigilance, Pharmaceutical Industry, Regulatory Requirements, GMP, FDA, Drug Development, Sop, Clinical Trials, Validation, Generic Programming
Experience
Principal advisor
Global Regulatory Affairs Advisors (GRA advisors)
Beijing, China
Chief Regulatory Affairs Officer
Overland Pharma
Beijing, China
Head, Regulatory Affairs Department
Pfizer
Beijing, China
Registration
Regualtory Affairs Director
Wyeth China
Beijing
Regulatory TA lead
Bristol Myers Squibb
Registration
Sr.Regulatory Manager
Pfizer China
Beijing City, China
Regualtory manager
GSK
Registration
Jie LI's Contact Information
Phone
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