Dr. Jiang is the founder of BioQingLam and the chief scientist of the R&D and industrialization of dissolvable MN TDDS. He granted his organic chemistry PhD from the Chinese Academy of Sciences.
He has been continuously focusing on R&D and industrialization of this DDS for many years, granted over 40 invention patents.
Dr. Jiang is a serial entrepreneur. Since his doctoral graduation in 2006, he has gained 6 complete experiences in the entire chain from R&D to industrialization, company governance, and ultimately achieving enterprise product sales.

Venus has more than ten years of experience in R&D, registration, and management of new drug formulations. She has served in multiple pharmaceuticals, responsible for the R&D, registration, and full lifecycle management for innovative drugs.
Venus is very familiar with the requirements of both research and registration for innovative drugs, especially the regulatory requirements of IND and NDA.

Olivia is an elite pharmacist. She is the 17th council member of GDPA, pharmaceutical engineering division, also a former CDE officer of China NMPA.
Olivia has almost 20 years’ experience for regulatory, supervision, and review. She served in several Chinese biotech and public companies as a senior regulatory role, leading more than 30 global regulatory campaigns while some of those are collaborated with Top 20 pharma such as Novartis and AstraZeneca.

XingYou is an experienced engineer with more than 15 years’ laboratory experience and worked in the quality department of pharmaceutical enterprises for more than 20 years. He is 3 times involved in the establishment inspection laboratory and also building up GMP system for 3 times. He is very familiar with ISO 9001、CNAS、WHO-PQ、EU GMP and FDA GMP, a truly veteran of GMP auditing profession.
XingYou has been engaged in the fields of biological products, traditional Chinese medicine preparations, chemical drug preparations, etc. for many years. Experienced quality research works for various forms of medicines, including but not limited to sterilized freeze-dried powder vials, liquid ambers, tablets, capsules, soft capsules, suspensions.

Tie Chen Director of factory Tie has over ten years of production management experience in big pharmaceuticals, specializing in the production process and technical management of sterile injections. He believes in the philosophy of lean production and performance management, and is proficient in quality, safety, and cost control. He has organized GMP certification for newly built workshops multiple times, and has also organized and participated in the re certification of EU GMP and the coordination of audits for Top 20 pharmaceutical companies.