
InnoStar's professional team ensured the reliability and integrity of the experimental data through a scientifically rigorous approach and highly efficient, precise technical operations. This provided critical data support for the successful clinical approval of Lutetium [177Lu]-BL-ARC001 Injection, accelerating the project's progress.
InnoStar Shanghai will be participating as a key partner at the 23rd SABPA BioPharma Conference, taking place on October 4, 2025, in San Diego, California.
August 11, 2025: NEUREGEN's NRG-103, the world's first in situ transdifferentiation-based gene therapy for glioblastoma, received FDA IND approval, with non-clinical support from InnoStar aiding the approval.
InnoStar and Cyberiad-Life developed a 3D-bioprinted mouse testicular organoid model, enabling in vitro reproductive toxicity screening, featured in ACS Biomater. Sci. Eng.
InnoStar launches its 24,000 sqm Nantong Phase II Non-Clinical Evaluation Platform in China, featuring 130 animal rooms to ease capacity constraints and accelerate drug development.
InnoStar Nantong Facility Successfully Passed U.S. FDA GLP Inspection
Copyright © 2017-2021©Shanghai InnoStar Bio-tech Co., Ltd. All Rights Reserved. Created By VPABrand.com