Experienced in nearly 20 years of drug development, familiar with CFDA, EMEA and FDA drug development regulations
Presided over the completion of more than 100 drug research and NDA
Presided over more than 20 new drug research and development projects，and obtained 15 clinical approval documents
Participated in a number of national "125" major special projects, "135" major new drug innovation and production projects
Published more than 20 articles in domestic pharmaceutical journals
Training minister of the alliance of Chinese pharmaceutical clinical trial institutions
Engaged in clinical trials of drugs and medical devices for nearly 20 years
Completed nearly 50 phases clinical trials of the drug
Completed nearly 30 clinical trials of medical devices
Presided over the accreditation work of GCP institutions in more than 50 hospitals；signed and completed phase I clinical trial with 5 institutions
Graduated from American university with a doctorate in Analytical Chemistry
Previously served in senior management positions at Merck BioRelianc, Frontier Biosciences, Eurofins, etc.
Rich experience in pharmaceutical research, clinical research and international registration projects
National Medical Products Administration new drugs evaluation expert
National Medical Products Administration drug GLP inspector
National Medical Products Administration medical device evaluation specialist
Doctor and researcher of the Academy of Military Medical Sciences
Worked on drug research and development institutions overseas for many years, presided over a number of new drug research and development projects in Canada, South Korea and other countries
Familiar with domestic and foreign drug policies and regulations, responsible for a number of domestic and foreign registered projects
Rich experience in biological products, Chinese medicine and chemical medicine research
Comprehensive experience in pre-clinical, clinical research, registration and declaration of new drugs
