Sysmex and J-TEC Sign a Research Collaboration Agreement Regarding Sterility Testing in Regenerative Medicine and Cell Therapy
Sysmex Corporation (HQ: Kobe, Japan; President: Kaoru Asano) and Japan Tissue Engineering Co., Ltd. (HQ: Gamagori, Aichi Prefecture; President & CEO: Ken-ichiro Hata; hereinafter “J-TEC” ) announced that they signed a research collaboration agreement regarding sterility testing in regenerative medicine and cell therapy (“the Agreement”) as part of strategic approaches based on the basic agreement* concluded in December 2024.
Sysmex aims to develop fast and safe sterility testing for regenerative medicine and cell therapy by applying its flow cytometry technology, where microscopic particles are passed through a flow channel for optical analysis of each particle as it flows, in collaboration with J-TEC’s expertise and knowledge.
* December 5, 2024 news release: “Sysmex and J-TEC Sign a Basic Agreement to Advance Manufacturing Capabilities for Regenerative Medicine and Cell Therapy” https://www.sysmex.co.jp/en/news/2024/241205.html
In regenerative medicine and cell therapy, because living cells are used as raw materials and because of individual differences in cells, quality control testing to ensure the safety and effectiveness of the products is extremely important. Particularly, sterility testing is important because viable cells can be a source of infection. Furthermore, expanding the scale of production and increasing efficiency are key issues in the regenerative medicine and cell therapy industry, and speeding up quality control testing is expected to help resolve these issues.
Against this background, the two companies concluded a research collaboration agreement in March 2025 to jointly develop quality control testing by combining Sysmex’s quality control inspection systems with J-TEC’s experience in developing and manufacturing regenerative medicine and other products.
Research conducted in collaboration with academia has suggested that Sysmex’s flow cytometry technology could be used for sterility testing in regenerative medicine and cell therapy, and the company plans to introduce its flow cytometry technology to the market (for research use) during fiscal 2025.
J-TEC will work to optimize Sysmex’s technology in light of J-TEC’s experience in manufacturing, developing and selling regenerative medicine and other products so that the technology can be introduced into such products.
If the joint research can demonstrate that flow cytometry technology provides equivalent sensitivity and rapid results compared to conventional methods, it is expected that sterility testing, which traditionally takes several weeks, could be shortened to just a few tens of minutes while maintaining product safety. The global market size for sterility testing in the manufacturing of regenerative, cell, and gene therapy products is estimated to reach approximately $280 million in 2022 and $1.36 billion by 2033.
Through this activity and new strategic themes being considered by both companies, Sysmex and J-TEC seek to resolve issues in quality control and other related areas of regenerative medicine and cell therapy, contributing to the development of a sustainable regenerative medicine and cell therapy industry in Japan.
- The purpose of this news release is to communicate our business activities to our stakeholders. It may or may not include information about Sysmex’s products or their research and development, but this is not intended for promotion, advertising or medical advice. The information contained in this news release is current as of the date of the announcement but may be subject to change without prior notice.