Live Stream Preview | From 1 to Infinity: Unlocking the Infinite Possibilities of Cell Culture!
Release Date:
2025-05-19 15:13

Shanghai Hycells Biotechnology is a biotechnology innovation company specializing in primary immune cell research, dedicated to providing customers with comprehensive, one-stop solutions for immune cells and stem cells. We offer compliant, ethically sound immune cell and stem cell collection services, while also launching High-quality, safe, and reliable HiXpan Registered trademark Serum-Free Culture Kit Series , empowering high-quality research on cellular biology and clinical applications. Hycells HiXpan Registered trademark We have achieved domestic production across the entire value chain for culture-based products, from biological raw materials to finished formulations, leveraging the domestic supply chain to build a complete industrial ecosystem. Our processes rigorously adhere to ISO standards for raw material selection, manufacturing management, and quality control. The resulting products enable the generation of immune cells with high purity and robust expansion efficiency, eliminating the need for feeder cells and thereby minimizing batch-to-batch variability and microbial contamination. Formulated without serum or animal-derived components, these products meet GMP and IND submission requirements, reducing regulatory risks.
On May 16, 2025, from 11:00 a.m. to 11:30 a.m., MedMai Premium will host a special live session on cutting-edge cell-culture products. Mr. Huang Xin, Product Technology Manager at Heyou Bio, will provide an in-depth analysis of the technical advantages of the HiXpan® product, covering everything from 1 to ∞, unlocking limitless possibilities for your cell culture!
Main Lecturer: Huang Xin
Co-founder & Product Technology Manager
Report Topic: Dual-Core Drive—NK and γδ T cells Innovations in Amplification Technology and the Future of the Industry
With nearly a decade of deep expertise in the field of cell therapy, the company is committed to technological innovation and its industrial application. It possesses end-to-end capabilities spanning from basic research to commercialization, with a keen understanding of emerging trends in the cell therapy industry. The team combines rigorous scientific thinking with a strong business orientation, excelling in building robust technology platforms and leading high-performing teams. In 2021, the company joined Hycells, where it was responsible for establishing the company’s technical and quality management systems, covering the entire workflow from cell preparation and quality control analysis to process development. The focus has been on optimizing primary cell manufacturing processes, developing standardized operating procedures, and significantly enhancing production efficiency and batch-to-batch consistency. This effort has resulted in multiple invention patents and utility model patents, thereby establishing core technological barriers. Prior to joining Hycells, the individual held positions at Vitong Lihua Laboratory Animal Technology Co., Ltd., where they solidified their foundation in cell culture and biological assay techniques, built cell isolation, preparation, and quality control platforms, and formulated standardized operating procedures. Standard Operating Procedure ).

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Compliance‑driven traceability establishes a clear “identity” for the product, but the real test lies in safety. While a multi‑donor pooling strategy ensures batch‑to‑batch consistency, it also inevitably elevates the risk of pathogen introduction. In the face of these associated risks and challenges, Heyousheng has never compromised on its manufacturing standards—relying on more precise design to deliver on its promise of enhanced safety.
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In selecting hPL raw materials, Heyousheng consistently upholds the principle that “safety is determined at the source.” The samples used in production are rigorously collected in accordance with applicable standards and undergo stringent donor screening, effectively mitigating the risk of disease transmission at the very outset. Moreover, from informed consent forms and ethical approvals to clinical‑grade collection under the GCP framework, Heyousheng has established a fully traceable documentation chain, ensuring that every sample is accounted for and verifiable. In contrast to the industry’s longstanding reliance on the conventional model of using expired blood supplies from blood banks, this approach represents a structural, generational upgrade.
