Consulting on Regenerative Medicine and Contract Cell Culture
First written in FY2016. 10 of 17 entries say "Restated". Latest entry: FY2024.
0 other companies' latest entry also says "Restated".
- FY2024RestatedAnnual report
「In addition, we provide consulting to providers of regenerative medicine and other medical services and contract manufacturing services for specified cell-processed products in accordance with the Act on the Safety of Regenerative Medicine and Other Products, which came into force in November 2014.」
The company continues to provide consulting to providers of regenerative medicine and other medical services and contract manufacturing through its licensed cell processing facility. - FY2023-Q2RestatedAnnual report
「Under the Act on the Safety of Regenerative Medicine and Other Products, we provide consulting to providers of regenerative medicine and other medical services, as well as contract manufacturing services for specified cell-processed products.」
The company continues to provide consulting to providers of regenerative medicine and other medical services and contract manufacturing of specified cell-processed products. - FY2023-Q1RestatedAnnual report
「Under the Act on the Safety of Regenerative Medicine and Other Products, we provide consulting to providers of regenerative medicine and other medical services, as well as contract manufacturing services for specified cell-processed products. Our consulting services support the administrative procedures required for clinical research and the provision of treatment, including preparing plans for the provision of regenerative medicine and other medical services and establishing operating systems for cell processing facilities. Under our contract manufacturing service for specified cell-processed products, we accept contracts to manufacture specified cell-processed products at our cell culture and processing facility licensed by the Ministry of Health, Labour and Welfare.」
The company continues to provide consulting to providers of regenerative medicine and other medical services and contract manufacturing through its licensed cell culture and processing facility. - FY2022-Q1RestatedAnnual report
「Under the Act on the Safety of Regenerative Medicine and Other Products, we provide consulting to providers of regenerative medicine and other medical services, as well as contract manufacturing services for specified cell-processed products.」
The company continues to provide consulting to providers of regenerative medicine and other medical services and contract manufacturing of specified cell-processed products at its licensed cell processing facility. - FY2021-Q2RestatedAnnual report
「Under the Act on the Safety of Regenerative Medicine and Other Products, we provide consulting to providers of regenerative medicine and other medical services, as well as contract manufacturing services for specified cell-processed products. Our consulting services support the administrative procedures required for clinical research and the provision of treatment, including preparing plans for the provision of regenerative medicine and other medical services and establishing operating systems for cell processing facilities. Under our contract manufacturing service for specified cell-processed products, we accept contracts to manufacture specified cell-processed products at our cell processing facility licensed by the Ministry of Health, Labour and Welfare.」
The company continues to provide consulting to providers of regenerative medicine and other medical services and contract manufacturing of specified cell-processed products at its licensed cell processing facility. - FY2020RestatedAnnual report
「We provide consulting to providers of regenerative medicine and other medical services, as well as contract manufacturing services for specified cell-processed products.」
The company continues to provide consulting to providers of regenerative medicine and other medical services and contract manufacturing through its licensed cell processing facility. - FY2020-Q3RestatedAnnual report
「Under the Act on the Safety of Regenerative Medicine and Other Products, we provide consulting to providers of regenerative medicine and other medical services, as well as contract manufacturing services for specified cell-processed products. Our consulting services support the administrative procedures required for clinical research and the provision of treatment, including preparing plans for the provision of regenerative medicine and other medical services and establishing operating systems for cell processing facilities. Under our contract manufacturing service for specified cell-processed products, we accept contracts to manufacture specified cell-processed products at our cell processing facility licensed by the Ministry of Health, Labour and Welfare.」
The company continues to provide consulting to providers of regenerative medicine and other medical services and contract manufacturing through its licensed cell processing facility. - FY2020-Q2RestatedAnnual report
「Under the Act on the Safety of Regenerative Medicine and Other Products, we provide consulting to providers of regenerative medicine and other medical services, as well as contract manufacturing services for specified cell-processed products. Our consulting services support the administrative procedures required for clinical research and the provision of treatment, including preparing plans for the provision of regenerative medicine and other medical services and establishing operating systems for cell processing facilities. Under our contract manufacturing service for specified cell-processed products, we accept contracts to manufacture specified cell-processed products at our cell processing facility licensed by the Ministry of Health, Labour and Welfare.」
The company continues to provide consulting to providers of regenerative medicine and other medical services and contract manufacturing of specified cell-processed products at its licensed cell processing facility. - FY2020-Q1AdvancedAnnual report
「Revenue from the regenerative medicine contract business for the cumulative first quarter was ¥124.185 million, up 40.5% year on year. Revenue increased from the same period of the previous year due to milestone income and other revenue associated with advancing contracted projects. In March 2019, Gamagori City Hospital joined the joint research facilities for clinical research treating vitiligo and intractable skin ulcers at Nagoya City University Hospital, enabling us to accept contract manufacturing of cultured epidermis from the hospital from April of the same year.」
Revenue from the regenerative medicine contract business increased 40.5% year on year, with milestone income recognised as contracted projects progressed. Contract manufacturing of cultured epidermis for Gamagori City Hospital also became available from April 2019. - FY2019AdvancedAnnual report
「In March 2019, Gamagori City Hospital joined the joint research facilities for this clinical research, and we will proceed with contract manufacturing of the same epidermis for the hospital.」
For contract manufacturing of cultured epidermis, Gamagori City Hospital joined the clinical research at Nagoya City University Hospital as a joint research facility, advancing the expansion of contract customers. - FY2019-Q3AdvancedAnnual report
「Revenue from the regenerative medicine contract business for the cumulative third quarter was ¥473.520 million, up 15.3% year on year. The number of contracted customers increased in response to growing corporate activity in regenerative medicine and other areas. Revenue was also supported by milestone payments received as contracted research projects reached milestones, as well as increased new orders for development consulting and contract development and manufacturing of regenerative medicine products.」
The regenerative medicine contract business increased its number of contracted customers, milestone receipts, and new orders, resulting in a 15.3% year-on-year increase in revenue. - FY2019-Q2AdvancedAnnual report
「Revenue from the regenerative medicine contract business for the cumulative second quarter was ¥297.651 million, up 21.3% year on year.」
Revenue from the regenerative medicine contract business increased 21.3% year on year, reflecting the expansion of development consulting, contract development and manufacturing, and contract manufacturing of cultured epidermis. - FY2018-Q3RestatedAnnual report
「Under the Act on the Safety of Regenerative Medicine and Other Products, which came into force in November 2014, we provide consulting to providers of regenerative medicine and other medical services, as well as contract manufacturing services for specified cell-processed products.」
The company continues to provide consulting to providers of regenerative medicine and other medical services and contract manufacturing of specified cell-processed products. - FY2018-Q2AdvancedAnnual report
「In July 2017, under the Act on the Safety of Regenerative Medicine and Other Products, we secured contracts from medical institutions and other organisations to manufacture specified cell-processed products, including cultured epidermis for use in clinical research treating vitiligo and intractable skin ulcers at Nagoya City University Hospital. We also newly secured several contracts to support the preparation of treatment provision plans and to provide consulting on the construction and operation of manufacturing facilities.」
The company secured a contract to manufacture cultured epidermis for Nagoya City University Hospital and several consulting contracts relating to the preparation of treatment provision plans and the construction and operation of manufacturing facilities. - FY2018-Q1AdvancedAnnual report
「We also proceeded with preparations from July 2017 for contract manufacturing for cultured epidermis transplants at Nagoya City University Hospital for conditions including vitiligo and intractable skin ulcers.」
Preparations have progressed for beginning, in July 2017, contract manufacturing for cultured epidermis transplants for Nagoya City University Hospital under contracts to manufacture specified cell-processed products. - FY2017-Q1RestatedAnnual report
「Following the enforcement of the Act on the Safety of Regenerative Medicine and Other Products in November 2014, we launched a consulting business for providers of regenerative medicine and other medical services and cell processing and manufacturing operators, as well as a contract cell culture business. In October 2015, we obtained a licence to manufacture specified cell-processed products, establishing the framework to accept cell culture contracts from medical institutions and other organisations.」
The company continues to provide regulatory compliance consulting related to regenerative medicine and contract cell culture services. - FY2016First statedAnnual report
「We launched a regulatory compliance consulting business for providers of regenerative medicine and other medical services, as well as cell processing and manufacturing operators, using the expertise we had developed through our regenerative medicine products business. In October 2015, we obtained a licence to manufacture specified cell-processed products and launched a contract cell processing business for medical institutions and other organisations.」
The company is applying its expertise in complying with the Act on the Safety of Regenerative Medicine and Other Products to new businesses in consulting and contract cell culture.