Bringing Global Compliance Standards to Chinese Pharmaceutical Packaging

Fully automated high-speed continuous production lines cover 15 core processes, with more than 60 quality control nodes and over 20 key control indicators, plus an AI in-line quality control system for real-time monitoring of the production process. The continuity of the inner coating is controlled below 20mA, and the total microbial limit is controlled within 30 cfu/tube. Element impurities such as arsenic, mercury, lead, cadmium, cobalt, nickel, vanadium, chromium, copper, molybdenum and aluminum as well as solvent residues are strictly controlled; insoluble particles are strictly controlled.

Shunfeng Pharma Packaging relies on the Packaging Materials and Containers Testing Center of the Guangdong Medical Devices Quality Surveillance and Inspection Institute (the packaging center). With an authoritative research platform, standard system and testing technology strength, the company has long carried out technical work such as new product and new material development tests, compatibility studies of pharmaceutical packaging materials, product testing and fundamental material research, and continuously receives authoritative official technical consulting, standard interpretation, regulatory guidance and professional testing technology training.

All core inspection, R&D and technical personnel of the company have received professional training at the packaging materials center and passed assessments, possessing standardized hands-on capabilities and compliant professional standards, with all staff certified for their posts. Relying on authoritative technical empowerment and a standardized control system, the company achieves standardized and regulated control over the whole process from material R&D, product testing and quality inspection to compliance system operation, ensuring all testing data is authentic, accurate, traceable and fully compliant with national pharmacopoeia requirements as well as relevant regulations and industry standards for pharmaceutical packaging materials.

We provide reverse research services for the primary packaging of generic drugs, analyzing the key materials and parameters of reference aluminum tubes and defining the core quality indicators of the packaging system, providing complete data support for your formulation R&D, packaging selection and associated filing, helping to narrow the quality gap with reference packaging and efficiently advance generic consistency evaluation and filing.