Sinofn Health
Sinofn Health
At SINOFN Health, we specialize in advanced Suspension Dosage Form manufacturing. Unlike traditional tablets or hard capsules, suspension technology offers superior bioavailability and patient compliance. As global dietary supplement brands shift toward "medical-grade nutrition," the ability to stabilize active ingredients in liquid suspension is a critical competitive advantage.
Our ODM processes leverage deep R&D, focusing on particle size reduction, surfactant optimization, and taste masking, ensuring that your final product is not only effective but also highly palatable for consumers. By partnering with us, you gain access to the Chinese Academy of Sciences (CAS) backed formulations, setting your brand apart in the crowded global supplement market.
Our Tianjin R&D and manufacturing hub utilizes massive scale efficiencies. We combine low-cost production with high-tech precision, allowing us to maintain competitive pricing while exceeding FDA/EU quality benchmarks.
We understand that a formulation approved in Asia may require adjustments for the US or EU markets. We provide regulatory consulting to navigate labeling, ingredient safety, and localization requirements.
ISO 22000, HACCP, and FSSC 22000 are just the baseline. Our quality management systems include blockchain-verified batch tracking, ensuring complete transparency from raw material sourcing to the final delivery.
Founded by Mrs. GuoHong Liu in 2012, SINOFN was born from a mission to democratize specialized nutrition. This clinical background informs every aspect of our R&D. Our team, led by Dr. Zhang Ying (CAS Postdoc) and Dr. Tan Shengjie (Peking University Medical Doctor), bridges the gap between pharmaceutical research and commercial supplement manufacturing.
Dr. Tan Shengjie - 15+ years experience in metabolic formulations.
Dr. Zhang Ying - Specialized in bioactive compound delivery systems.
Hans van Dijk - EU regulatory specialist & expert in dosage technology.
Yes, we operate dedicated pilot-scale production lines. Whether you are an enterprise or a growing startup, we support rapid iterations of suspension and liquid dosage forms to test market feasibility before full-scale launches.
We implement a dual-gate quality system. First, internal testing using HPLC/GC-MS ensures strict adherence to specifications. Second, we work closely with your regional regulatory teams to ensure all formulations comply with the destination country's dietary supplement regulations (e.g., FDA for the US, EFSA for the EU).
