Production R&D
Anhui Bocompounds Pharmaceutical Co., Ltd Located in the Dongzhi Economic Development Zone of Chizhou, Anhui Province, it covers an area of 290 acres and is a wholly-owned subsidiary of Biocompounds Pharmaceutical Inc.
Relying on the background of its holding company Zhejiang Jianfeng Pharmaceutical Co., Ltd. (abbreviated as Jianfeng Pharmaceutical) and parent company Biocompounds Pharmaceutical Inc. (abbreviated as Bocompounds Pharmaceutical ), Anhui Bocompounds Pharmaceutical serves as the characteristic active pharmaceutical ingredient (API) base for Jianfeng Pharmaceutical to implement its "characteristic API + formulation" strategy. It is primarily engaged in the research and development, production, and sales of APIs and advanced intermediates.
Anhui Bocompounds Pharmaceutical focuses on the field of specialty active pharmaceutical ingredients (APIs) and advanced intermediates. Its main products include fluoroquinolone APIs and intermediates, tineidone APIs and intermediates, new mechanism acid-suppressing drugs - potassium ion competitive acid blockers (P-CAB for short) APIs and intermediates, antihypertensive APIs and intermediates, etc. Among them, the fluoroquinolone series of fluoxetine carboxylic acid is one of the world's leading manufacturers of quinolone APIs, with products selling well in domestic and overseas markets. The company is committed to becoming a well-known enterprise in the field of specialty APIs and advanced intermediates both domestically and internationally.
The company possesses advanced production equipment and technology, enabling it to efficiently produce high-quality products.
We attach great importance to technological innovation, continuously increase R&D investment, establish a high-quality technical R&D team, and actively collaborate with universities, CR0, and other research institutions to ensure the innovation and competitiveness of our products.
Through the integration of upstream and downstream industrial chains, a comprehensive supply chain system has been established, effectively reducing costs and enhancing the market competitiveness of enterprises.
Actively expand the market, pursue a leading position in the target market, and enhance market control through the growth of market share.
The company has obtained the cGMP quality management system certification, ensuring the safety, effectiveness, and controllability of its products.
In accordance with national safety management laws and regulations, a set of strict safety management systems and operating procedures have been established, equipped with advanced safety detection equipment and emergency response facilities. Systematic risk assessments have been conducted, and targeted preventive measures have been formulated to reduce the likelihood of accidents and mitigate potential safety risks.
In accordance with national laws and regulations on ecological environment management, we have established standardized environmental protection management systems and operating procedures. Through continuous technological innovation and the adoption of green processes, we achieve green and clean production. We invest in the construction of efficient environmental protection facilities such as wastewater treatment stations and exhaust gas treatment facilities, ensuring that emissions meet or exceed national emission standards.
The first phase of the project, with an investment of 150 million yuan, involves local technical renovation of the existing equipment and facilities in workshops 101 and 102, as well as auxiliary buildings, to form a production workshop capable of producing 1,200 tons of pharmaceutical intermediates such as levofloxacin carboxylic acid, ofloxacin carboxylic acid, moxifloxacin, and pefloxacin.
The second phase of the project, with an investment of 350 million yuan, has successfully established two GMP workshops and an independent hydrogenation workshop, capable of meeting various needs such as acylation, amination, cyclization, condensation, hydrolysis, hydrogenation, reduction, and cyanation. Currently, the company boasts a high-end manufacturing platform for active pharmaceutical ingredient (API) CMO/CDMO, with production lines for annual output of hundreds of tons of small molecule targeted anti-tumor drug APIs and their intermediates, as well as production lines for thousands of tons of APIs and advanced intermediates for cardiovascular, antidepressant, antiviral, and other drugs.

The wastewater treatment system is designed with a capacity of 1500T/D and equipped with advanced online monitoring equipment and automated control systems. It can continuously detect various indicators of wastewater and achieve intelligent management of the entire wastewater treatment process, ensuring efficient wastewater disposal and reducing operating costs.
Based on the properties of the exhaust gas, the company has conducted strict classification and disposal of the exhaust gas. Additionally, online monitoring equipment and automated control systems have been equipped on the exhaust gas disposal system to continuously monitor various indicators in the gas and intelligently dispose of it. The RTO incinerator, with an air volume of 20,000 m³/h, boasts high disposal efficiency, achieving a VOCs removal rate of over 99%.
The company has established a 420-square-meter hazardous waste storage facility in accordance with national regulations, capable of storing 200 tons of solid waste. It has also established a comprehensive management system and process for the entire process from the generation of solid waste to its disposal at the disposal unit.
Passed ISO9001 Quality Management System;
A scientific and comprehensive quality management system has been established in accordance with GMP, cGMP, and EUGMP standards;
Equipped with over 100 various analytical and testing instruments, primarily including 5 high-performance liquid chromatographs (from Agilent, Shimadzu, etc.) and 4 gas chromatographs (from Agilent, Shimadzu, etc.);
Share analytical equipment and testing resources with group subsidiaries;
Through audits of domestic and foreign customers and on-site inspections by the National Bureau;
A comprehensive audit and customer management system;
Pass GMP compliance inspection.