Hongjitang Pharmaceutical Quality Center has a history of over a hundred years and is a company specializing in pharmaceutical production. The company is committed to producing efficient, safe, and reliable medicines, always placing quality first, treating quality as the lifeline, and adhering to the principle of ‘one vote veto for quality issues.’ With a complete quality management system and comprehensive quality control system, the company has established a three-level quality assurance and document management system at the enterprise, workshop, and team levels, meeting the requirements of the latest GMP standards. This ensures that all employees fully comply with relevant regulations throughout the entire production process. The application of automation, information technology, and intelligent technology ensures process compliance, thereby guaranteeing effective and controllable product quality and safety.

Hongjitang Quality Management Platform covers an area of 1,600 square meters and has a team of more than 100 highly qualified professionals, over 90% of whom hold a bachelor’s degree or higher. The company is equipped with advanced testing equipment, including precision instruments such as GC, HPLC, UPLC, ICP-MS, LC-MS, GC-MS, IR, and UV. Impurity control is conducted by laboratories accredited by CNAS and CMA, ensuring the accuracy, traceability, and reliability of test data. The company has participated for ten consecutive years in the provincial pharmaceutical enterprise testing capability assessment organized by the Shandong Provincial Drug Administration. The assessment covers areas such as microbial testing and traceability, precise instrument content determination, heavy metal and harmful element residue testing, and physical property identification. The assessment results have consistently been ‘qualified,’ fully demonstrating the company’s excellent testing capabilities.

Hongjitang Pharmaceutical has established internal control standards for raw materials and products that exceed national standards to ensure product safety and efficacy. This enables the company to achieve comprehensive quality management and information traceability at all stages of the pharmaceutical lifecycle, from raw material procurement and production processes to finished product control and pharmacovigilance.