Milestones

May 1961,Mr.Te-Chung Huang established the Te-Chung Pharmaceutical Manufacturing Co., Ltd. in Huwei,Yulin.

November 1984, a new GMP-Standard factory in Donan was under construction. The company was then renamed "The Huang's Pharmaceutical Manufacturing Co., Ltd

"The Huang's" were transferred to the new factory in Donan.

Accredited by Department of Health (DOH) and by Industrial Development Bureau Ministry of Economic Affairs, the factory was approved the 70th G.M.P. Pharmaceutical Manufacturing Factory in Taiwan.

awarded the first GMP certificate in pharmaceutical manufacturing, same year, products were introduced to "省聯標 the invite public bidding," the greatest national medicine-request system, and the market was actively extended to VGH., NCKU Medical Center, and lots of private hospitals all over Taiwan.

the Office in Taipei was sited in Sec 4, Zhoung-Xiou East Rd, Taipei, in order to have a thorough understanding and expansion over the market.

the accomplishment of the computer network connecting Taipei and Donan helped realize the inteconnecting of marketing and qualification.

a special department of import, "Nature Power Co., ltd," was set in California and introduced customers to United States of America

the company set up [Telienl pharmacy Allianceine, expecting apothecaries] to exercise their knowledge. In April, "The Huang's [joined the Article Numbering Center of R.O.C.] to help managing the Huang's products.

The Huang's started the investment in [BE] experiments, Several products have passed the experiments now.

acording to the CGMP policy, the Huang's set up a group to secure the quality of manufacturing. January 1999, The "Quality Assure Validation Work Team" was set in response to CGMP policy. The adoption of "Validation Work" rules represents a higher level of Pharmaceutical Manufacturing technology

In February, The Huang participated in "Relief Fund Covered" as a leading role.

to manage the combination between market and production, The Huangs set a new project for more economic production structure.

the first-stage "Validation Working" was completed, then samples were soonsent to Medical Services Department of Health Executive Yuan Republic China and Mational Laboratories of Food and Drugs, Department of Health Exective Yuan, Republic of China, for examination.

under the evaluation of the CGMP evaluation team, The Huang's is recognized as the 11th company which has been qualified in CGMP on March,

the commendation awarded in Taichung by the burreau of public health gave a solid affirmation for the great improvement of The Huang's on pharmaceutical manufacturing technology. The commendation is a high-leveled certificate on the quality of the merchandises.

Established China Office in Shanghai to have a perspective future in the pharmaceutical market in Mainland China. In November, the company received the first enter the People's Republic of Representative Offices of Foreign (regional) business registration certificate.

hina Food and Drug Administration (CFDA) approved the first drug license, the Chairman Mr. Huang personally receive it in Beijing. Signed a distributor in import of sales to China contract with ZhongLu Medicines Ltd., export

Hwang’s Cetypridinium Chloride Buccal Tablets formal inputted in various medical sales channel in Fujian.

Pharmchina ( Xiamen )

China agent transferred from Shanghai ZhongLu Medicines Ltd to Shenzhen Rosso Pharmaceutical Co.Ltd.

With the government to implement PIC / S policy, Donan factory has an expansion project to add Hormones independent manufacturing factory.

Hwang’s Cetypridinium Chloride Buccal Tablets through the major clinical trial evaluating medical institutions

Actively pursued the expansion of the market in Southeast Asia to achieve the goal of exports

Applied Food and Drug Administration, Ministry of Health and Welfare PIC/S GMP inspection. In October hormonal preparations independent plant, certified by PIC/S GMP of international standard evaluation.

Hwang’s Pharmaceutical becomes an international PIC/S GMP certified factory specifications, pharmaceutical standards and verification specification with the world.

With the GDP Policy, construction of a new warehouse in order to achieve the GDP Policy, and clearly control the quality medicine after distribution after the factory.

Accreditation Certificate of Foreign Drug Manufacturer approved by The Ministry of Health, Labour and Welfare in Japan.

Received an expanded subsidy from the Invest Taiwan of the Ministry of Economic Affairs to invest in a new PIC/S GMP-grade plant to continue to increase production capacity.