MILESTONE
~ORIGIN~
Team work to build Chinese herbal biotechnical kingdom
1990-
Li Kang founder, Mr. Cheng, Ching-Hsiang, opened a Traditional Chinese Medicine clinic and a Chinese herbal medicine store in 1972. He continued to explore and study the essence of Traditional Chinese Medicine. After years of research and experience, he felt that the pharmaceutical industry was a conscientious cause that benefited the world. To promote the unique medical essence of Traditional Chinese Medicine and integrate it with modern biotechnology, and to expand production scale to benefit more people, he established Shengchuntang Pharmaceutical Industry Co., Ltd. in Yongkang Industrial Park, Tainan in 1982, and founded Likang Biotechnology Co., Ltd. in 1990.
2004-
Li Kang Biotechnical Co., Ltd was approved for "Chemical Products Manufacturing License Registration" with a capital of NT$100 million.
2007-
■August:Approval as a GMP pharmaceutical factory .
■September: Approved for chemical product manufacturing and pharmaceutical manufacturing. The factory site area is 11,352 square meters, with a building area of 7,135.78 square meters.
■October: Approved for food manufacturing and beverage manufacturing, including other foods, non-alcoholic beverages, cleaning products (general grade and food grade), and pharmaceuticals (NSAID Patches). The factory site area is 13,653.86 square meters, with a building area of 7,135.78 square meters.
2008-
The Medicine factory has been approved by "cGMP Good Manufacturing Practice" (patch dosage form).
2009-
■January: The Chinese medicine factory was audited and certified by the Department of Health, Executive Yuan, Taiwan, as a new plant with cGMP software, complying with Good Manufacturing Practice (GMP) regulations for pharmaceuticals. It also approved concentrated Chinese medicine dosage forms and general Chinese medicine dosage forms (a total of 23 types).
■November: The Li Kang Cultural Hall for Chinese herbs Industry was approved by the Industrial Development Bureau of the Ministry of Economic Affairs of Taiwan .
2012-
The Pharmaceutical Factory has been approved by the Taiwan Food and Drug Administration (TFDA) as a PIC/S GMP Certified professional patch manufacturer.
2017-
The medical device factory has been approved the ISO 13485 medical device quality management system certification.
2023-
The Chinese medicine factory was approved for the second phase of efficacy verification .
2025-
The medical device factory has been approved QMS (Quality Management System) certification from the Ministry of Health and Welfare.