At NINGBO INNO PHARMCHEM CO.,LTD., we understand that the production of pharmaceutical grade gelatin demands an unwavering commitment to quality and safety. The stringent requirements of the pharmaceutical industry necessitate adherence to rigorous standards throughout the entire manufacturing process.

Our production of pharmaceutical gelatin begins with the careful selection of raw materials, typically animal skins and bones, which are processed to extract high-quality collagen. This collagen is then converted into gelatin through controlled extraction methods. Throughout this process, meticulous attention is paid to maintaining purity and minimizing contamination. Compliance with Good Manufacturing Practices (GMP) is fundamental, ensuring that every step, from raw material handling to final packaging, is conducted under strict hygienic conditions.

Key quality control measures are implemented at various stages. This includes rigorous testing for chemical purity, microbial limits, heavy metals, and endotoxins. The characteristic properties of gelatin, such as bloom strength, viscosity, pH, and transparency, are precisely measured and controlled to meet pharmacopoeia specifications (e.g., USP, EP). These parameters are vital for ensuring consistent performance in downstream pharmaceutical applications, whether it's for the precise gelling required in capsules or the binding strength needed for tablets.

Traceability is another cornerstone of our quality assurance. Each batch of pharmaceutical gelatin can be traced back to its raw material source, providing transparency and accountability. This comprehensive approach to quality control ensures that the pharmaceutical gelatin supplied by NINGBO INNO PHARMCHEM CO.,LTD. is not only safe and effective but also consistently meets the high expectations of the pharmaceutical sector. By prioritizing these production standards, we aim to be a trusted partner for all your pharmaceutical ingredient needs.