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R&D

A well-established research and innovation platform

● National Postdoctoral Research Station in China.
● Provincial Engineering and Technology Research Center.
● Postdoctoral Innovation Practice Base, Postdoctoral Workstation, Enterprise Technology Center, and other research and innovation platforms.

Professional R&D team with expertise in drug-loaded lipid emulsions

● More than 20% of JIABO 's workforce, with 90% of R&D personnel holding a bachelor's degree or higher.
● Extensive experience in R&D, and industrialization of drug-loaded lipid emulsions.
● Rich experience in R&D, and industrialization of parenteral nutrition products.
● Experience in R&D of complex injectables, including liposomes.

First-class quality control system and production facilities

● Equipped with ultra-high-performance liquid chromatography (UHPLC) systems from brands like Agilent.
● Precision instruments such as internationally renowned brands of liquid chromatography-mass spectrometry (LC-MS), gas chromatography-mass spectrometry (GC-MS), and ICP-MS.
● Homogenizers and other equipment related to the development and production of lipid emulsions.

A rich portfolio of R&D patents and independent research projects

● A total of 40 invention patents, 3 utility model patents, and 2 design patents have been granted.
● The invention patent for ‘Preparation Method of Propofol MCT/LCT Injection’ won the National Patent Excellence Award.
● 35 self-developed R&D projects have been undertaken, in addition to 1 national project, 7 provincial-level science and technology projects, and 8 municipal-level science and technology projects.

MANUFACTURING FACILITIES

JIABO is strategically located within the "One-Hour Living Circle" of the Pearl River Delta, approximately 70 kilometers from the center of Guangzhou. It takes just 20 minutes to reach the Qingyuan High-Speed Rail Station, which connects to Guangzhou South Station, and is close to the Guangqing Intercity Station, offering direct access to Guangzhou Baiyun Airport within one hour.

JIABO operates 10 GMP-certified production lines, including those for small-volume and large-volume injectables, sterile small-volume injectables, soft bag lines, and APIs, capable of meeting the industrial-scale production requirements for various complex injectable formulations.

Additionally, JIABO has a specially designed production line that meets EU standards and is in the process of applying for EU GMP certification to enhance its competitive position.

COMPLIANCE

Good Manufacturing Practice(GMP)

Adhering to the principle of Quality First: 
Committed to improving product quality control throughout the production process to ensure that the output meets regulatory requirements and intended use.
 
JIABO has fulfilled its quality objective of ensuring a 100% pass rate for all products released. With a newly built production line meeting EU/FDA/WHO GMP standards, are set to enter high-regulation markets in the coming year.

Implementing the 6S management system(SEIRI、SEITON、SEISO、SEIKETSU、SHITSUKE、SECURITY): 
Promoting the overall management level and efficiency of the production site, striving to align with international first-class standards.

Quality Management System(QMS)

JIABO focuses on quality and innovation, adhering to ‘Quality First’ policy. The company has established a comprehensive quality management system in compliance with international standards and has introduced advanced inspection equipment. The internal quality control standards for all JIABO products exceed national requirements. In September 2011, JIABO was invited to draft the national unified standard for ‘Propofol Injection’, which was officially implemented in 2016.

JIABO's APIs and FDFs have all passed the updated national GMP certification, with the Propofol API also receiving EU CEP certification. The company's FDFs are exported to over 15 countries and regions, and its overall quality management ranks among the best in the domestic pharmaceutical industry.

Pharmacovigilance(PV)

Our company has established a pharmacovigilance system in compliance with China’s Pharmacovigilance Quality Management Standards and regulations. A Drug Safety Committee, led by the legal representative and comprising the pharmacovigilance officer and relevant staff, oversees major risks, safety incidents, and risk control decisions.

An independent pharmacovigilance department is responsible for the system’s development and implementation. The pharmacovigilance officer, appointed by the legal representative, is trained in applicable laws and regulations.

We leverage advanced systems, including China’s Adverse Drug Reaction Direct Reporting System and the Insight Pharmacovigilance Electronic System.

Environment、Health、Safety(EHS)

Environmental Management: The company complies with national regulations, focusing on pollution prevention, clean production, and waste reduction. We ensure compliant emissions, minimize energy consumption, and strive for a ‘green, zero-waste factory’ to promote sustainability.

Occupational Health Management: Aligned with the Occupational Disease Prevention and Control Law, we prioritize hazard prevention and employee health. Our comprehensive approach safeguards employ well-being, enhances productivity, and improves our reputation.

Safety Management: Safety is paramount. We implement preventive measures, engage employees, and cultivate a safety-first culture to ensure secure operations and sustainable growth.

Fire Safety Management: We comply with fire safety laws, emphasizing prevention and emergency preparedness. By enhancing awareness and response capabilities, we protect lives, assets, and support long-term development.
Welcome to inquire and look forward to working with you Have any inquiries or 
make phone calls +86-763-3299260

QUICK LINKS

PRODUCTS CATEGORY

CONTACT US

 +86-763-3299260
 Overseas Sales Dept.
overseas@jiabopharm.com
 +86 1385 388 6472
 Bio-Pharmaceutical Park, High&New Technology Industry Development Zone, Qingyuan, Guangdong Province, China

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