The radioisotope platform provides comprehensive capabilities for the non-clinical and clinical evaluation of radiopharmaceuticals and radioisotope-labeled compounds. With the qualification to use 36 different radioisotopes, the platform supports a range of studies, including ADME research, human material balance studies, molecular imaging, and radiopharmaceutical evaluations. The platform is equipped with state-of-the-art experimental facilities and equipment, including a γ counter, liquid scintillation counter, QWBA, PET/MR imaging, and other advanced testing technologies. It supports a variety of animal models, including mouse, rat, rabbit, dog, pig, and non-human primates, and provides end-to-end analysis of radioactive biological samples.
Certified by NMPA, OECD, and FDA, the platform strictly follows GLP/GCP international standards, providing whole-process solutions that meet global standards for innovative drug development. The platform's capabilities are bolstered by its three-dimensional advantages of qualification, hardware, and technology.
Radioactive class B sites
Qualified to use 31 different isotopes
Platform Qualification
The platform holds qualifications for 36 different radioactive isotopes, making it one of the few institutions with such a broad spectrum of isotope use qualifications.
Comprehensive Research Capability
The platform offers simultaneous ADME studies (absorption, distribution, metabolism, excretion) of 3H/14C labeled compounds, human material balance studies, live molecular imaging, and both non-clinical and clinical evaluations of radiopharmaceuticals.
One-Stop Service
The platform supports the full process of radioactive clinical biological sample analysis—from sample collection and processing to analysis—providing complete and accurate data support for clinical research. This integrated approach helps to streamline the clinical stage research of drug development and reduces the cost associated with cross-platform collaborations.
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