COMPANY PROFILE

Drug quality and safety informatization expert

Zhuhai Feiqi Yaodian Technology Co., Ltd. (hereinafter referred to as Feiqi Yaodian) is the former digital pharmaceutical division of Guangdong Feiqi Internet Technology Co., Ltd. in order to better create a professional brand in the pharmaceutical industry, it has established a holding subsidiary. Founded in 2009, Feiqi Internet is an innovative enterprise on the new third board (Stock Code: 834791), with a registered capital of 32.49 million yuan, nearly 400 employees and a sales revenue of 236 million yuan in 2020.

Headquartered in Zhuhai national high tech Industrial Development Zone, the company has set up molecular companies in Beijing, Shanghai, Chongqing, Shenzhen and other places. It has more than 300 industrial chain partners in China. It is a national high-tech enterprise guided by technology. It is the best application brand of GMP management software recommended by the quality authorized person association and Guangdong Pharmaceutical Association, "double soft certification" enterprise. In the same industry, it took the lead in passing ISO9002 quality management system certification and CMMI5 international authoritative certification.

Relying on the strong technical support and industrial chain advantages of flying enterprise interconnection, flying enterprise Yaodian takes wisdom, green and safety as its business philosophy and takes the digitization of quality management in the pharmaceutical industry as its main business. At present, it has formed three business forms: digital service, intelligent service and consulting service.

Yaodian technology is committed to building a digital and intelligent operation and management platform for tracing the quality of the whole industrial chain of pharmaceutical enterprises.

According to the quality management requirements of the international organization for Standardization (ISO), the World Health Organization (who), the International Pharmaceutical Engineering Association (ISPE) and relevant GMP regulations at home and abroad for the drug life cycle, the customized and developed total quality information management platform covers the R & D, testing, production and quality of pharmaceutical enterprises.

Yaodian technology is the only information construction enterprise in China with the overall solution of the whole ecological chain of pharmaceutical product R & D and quality management (LIMS, QMS, DMS, TMS and PMS).

TEAM
It has a team that goes deep into the pharmaceutical industry and has professional and comprehensive information related system construction in the pharmaceutical industry!
General manager Li mengke

Senior industry expert, visiting lecturer of dandelion, with more than ten years of experience in the R & D and implementation of quality management software in the pharmaceutical industry, in-depth understanding and practice of CGMP regulations and CSV verification system, is a pioneer in cGMP management software in the domestic software industry.

Once served as R & D, implementation and consulting of LIMS, QMS, DMS, TMS, PMS and other projects in the pharmaceutical industry, mainly responsible for large pharmaceutical group projects such as Lizhu group, Tongrentang, China Resources Sanjiu, Sanjin pharmaceutical, Taiji group, Yiling pharmaceutical, amendment pharmaceutical, Lukang Pharmaceutical, North China Pharmaceutical, East Sunshine pharmaceutical and so on.

Deputy general manager and chief designer Dr. Jimmy Zeng

He majored in chemistry, postdoctoral fellow of City University of New York, President of American Chinese Professionals Association, worked in Baxter and Purdue pharmaceutical companies in the United States, one of the top 50 global pharmaceutical companies for 18 years, and served as senior researcher and deputy director of R & D analysis.

After returning to China in 2013, he worked as a part-time senior quality technical consultant and chief scientist in Zhendong pharmaceutical, Jiangsu Hengrui pharmaceutical, Beijing Shiqiao biology and other pharmaceutical companies. He has worked in American and Chinese pharmaceutical companies for nearly 30 years and has rich experience in international ICH, cGMP, USP guidelines, quality QA system, analysis and quality control, QC laboratory management, research project initiation and project promotion, international business development, BD and other fields. One of the few successful experts who participated in the successful research and development of three new drug NDA projects for 15 years, participated in the whole process research and development in the United States and applied for listing in the United States. One NDA product has an annual sales of more than US $1 billion. At present, he is the deputy general manager and chief designer of Feiqi Internet and the general consultant of pharmaceutical enterprise projects such as Tongrentang and North China Pharmaceutical. He integrates many years of American pharmaceutical laboratory experience with Feiqi software products to create more internationally competitive software products in the pharmaceutical industry.

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