Jinhe Biotechnology Co., Ltd. (Stock Code: 002688.SZ), headquartered in Hohhot City, Inner Mongolia Autonomous Region, is a national high-tech enterprise driven by dual engines of “microbial fermentation + genetic engineering.” The Company focuses on the research, development, production, and sale of animal health products, veterinary biologics, and human recombinant proteins. It was listed on the Shenzhen Stock Exchange in 2012. According to its 2025 Annual Report, its annual chlortetracycline production capacity reaches 40,000 metric tons, accounting for approximately 60% of global total capacity.  

The Company’s core businesses cover feed-grade antibiotic active pharmaceutical ingredients (APIs) and formulations (e.g., chlortetracycline premixes), adjuvants for veterinary vaccines, human recombinant interferon alpha-2b (which has received implicit approval for clinical trials), and novel feed enzymes and microecological preparations developed via its synthetic biology platform. Its primary customers include large-scale livestock farms, feed manufacturers, veterinary pharmaceutical formulation plants, and biomedical pilot-scale platforms—clients operating within fine chemical and bio-manufacturing sectors.  

Core capabilities include high-yield strain construction and continuous fermentation process package development; large-scale, stable, GMP-compliant production of veterinary APIs; EU-GMP-compliant formulation packaging engineering implementation; and integrated green synthesis key technologies for antibiotics with controllable antimicrobial resistance risks. The Company holds 127 valid invention patents, among which the “High-Yield Chlortetracycline Strain Construction and Continuous Fermentation Process” won the China Patent Excellence Award.  

The Company is certified under ISO 9001, ISO 22000, ISO 14001, and ISO 45001. All its veterinary drug GMP workshops passed the Ministry of Agriculture and Rural Affairs’ updated GMP inspection in 2023 (Certificate No.: (2023) Veterinary Drug GMP Certificate No. 178). Its human recombinant protein pilot-scale platform holds the National Medical Products Administration’s “Pharmaceutical Production License” (Category Code: Bh) and the European Directorate for the Quality of Medicines & HealthCare (EDQM) Certificate of a Suitability of Monograph to the European Pharmacopoeia (CEP) (R0-CEP 2022-117-M).  

Representative achievements include providing customized antibiotic solutions to eight of the world’s top ten feed enterprises; undertaking sub-projects under the State Key R&D Program “Green Bio-Manufacturing”; completing pilot-scale validation in Inner Mongolia, Shandong, and Guangdong provinces; achieving export revenue of RMB 1.28 billion in 2025, representing 37.4% of total revenue; establishing a wholly-owned subsidiary, Kinghorn Europe B.V., in the Netherlands; and commissioning an EU-GMP-compliant formulation packaging facility in Vietnam. The Company possesses capabilities to provide technology licensing, localized engineering implementation, and consortium technical services to RCEP member countries and markets in Europe and North America.