My name is Yang Shuqing. I was born on August 16, 1978 and live in Ya'an in Sichuan. I belong to the Han nationality. In 1998 I graduated from the Sichuan Electronic Science and Technology University.My major is Electromechanical-Integration. And the qualification is undergraduate.

Since April 1997 I was in Chengdu Kanghong Pharmaceutical Co., Ltd. for practice. During the practice I studied Chinese medicine from the pharmaceutical production process. Through the verification I renovate technical of the production process. This renovation has achieved good results and to follow the production so far.

After the expiry of practice I recognized by the leadership of the company and continue to work in Kanghong.

From February to April 1998, I was sent to Chongqing Ge Lansu pharmaceutical company for GMP certification training, and has achieved national GMP training certificates. In May and June 1998 I in the Chongqing Institute of Pharmaceutical Industry studied chemical production and management. Return to the company, I worked in the Department of Production Technology as GMP Certification Coordinator, and smoothly through the national GMP certification inspection in December.

In 1999 the company set up workshop for chemical raw materials,and I am deputy director of the workshop. Early I was in charge of projects-construction. After workshop completed, I mainly responsible for day-to-day production and certification information management. In April 2000 I smoothly through the national GMP certification examination of the chemical production.

In May 2000 I transferred to the machine-repair workshop as equipment manager.

In December 2000 I transferred to the Department of Production-Technology as Assistant manager, and I am responsible for all the hardware and equipment management and maintenance in the production base.

In November 2001 contract expires between I and Kang Hong pharmaceutical. In order to seek new space for development, I leave Kang Hong and as equipment management in Engineering Department of Tibet Pharmaceutical.

In November 2001, I worked in the Project-Construction agencies. I establish a good relationship of cooperation with the relevant government departments.

In November 2002, I was transferred to Lhasa, Tibet branch company in charge of production management and production technology, and I am concurrently the supply branch manager. During the work in Tibet, I have established good working relations and profound friendship with Tibet people and government departments.

In January 2004 I transferred back to Chengdu Branch and as equipment manager in the Engineering Department. I was responsible for equipment installation, commissioning and inspection work.

In May 2004 I again transferred to the Tibet branch and is responsible for engineering work. Because of illness and highland climate and other factors, in February 2005 I resigned to return to Chengdu.

In March 2005 to April 2006, I was deputy director of the Engineering Department in Sichuan Three-QiPharmaceutical Co., Ltd., and general manager of Special Assistant. During the work, I renovate technical of the artemisinin production line and have achieved good results in subsidiary- Chongqing Three-Qi artesunate development Co., Ltd.. The technology was in a leading position of the international high-risk technology. It was known as "the domestic forerunner" by peer. I kept close contact about artemisinin with Mr. Li Xiandong, who is as Managing Director of Switzerland Nuo Hua Group in China, and China Tianwei Group.

“Uphold the technological revolution, Capture the market opportunity” as the driving force to a .In the process of the search, and explore, at the invitation of Sichuan Yu Tuo Tibetan-Medicine pharmaceutical Co., Ltd I joined the company. I am as engineering manager in the company. In August 2006 I had the honour of becoming the member of the european delegation. I conducted a 43 day business visits and learning to United Kingdom. During the inspection, I studied " The Law Bill of EU Trade" and " Registered Law" in United Kingdom. On the products to enter the European market, I have a more profound understanding. In December, while my organization the Aba Red pharmaceutical company smoothly through the national GMP acceptance. In February 2007, I was appointed as the deputy general manager of Jiuzhai knife party company. I mainly responsible for import and export of medicine and sales.

In May 2007, at the invitation of a biotechnology company in Tibet(as the working, not be disclosed), I assist in the completion of the construction and certification of production lines. The standard of construction is in accordance with the EU FDA pharmaceutical standards. As far as possible by the end of 2008 the building is completed and certified. (The production line is mainly for the production of health, and adopt the international-advanced powder technology. It ensure maximum absorption rate of the human body.)