Supporting Innovative Radiopharmaceutical Bioanalysis and Radiolabeled Human AME Studies
Teddy’s Radiopharmaceutical Bioanalysis Platform has established a dedicated radiopharmaceutical laboratory of over 30 m² in Wuxi and holds a Class II Radiation Safety License. The laboratory is approved for handling up to 10 radionuclides, including C-14, Cu-64, Zr-89, Y-90, In-111, I-131, Lu-177, Pb-212, Ac-225, and Th-227, enabling sponsors to access comprehensive, one-stop services for innovative radiopharmaceutical development.
The
platform is equipped with gamma counters, liquid scintillation counters, and
online HPLC radio-detection systems, providing integrated capabilities for
pharmacokinetic studies, dosimetry assessment, urinary excretion analysis, and
data interpretation to support clinical research of novel radiopharmaceuticals.
Teddy
is supported by an experienced team of radiopharmaceutical laboratory
specialists and can deploy qualified technical staff to nuclear medicine
departments as required, delivering on-site testing and related technical
support services.
In addition, the radiopharmaceutical laboratory offers radiolabeled human AME studies for innovative drugs, including mass balance assessment, radioactive pharmacokinetics, metabolite profiling, metabolite identification, and non-radiolabeled pharmacokinetic analysis.
-
2000+
Central Lab Test Menu
-
480+
Laboratory Developed Test
-
6+
CAP Accreditations
-
1100+
Clinical Trials
Comprehensive Lab Service Capability
- Central laboratory
- Genomics
- Pathology
- Routine Test
- Flow Cytometry
- Bioanalysis
- Large molecule Bioanalysis
- Small molecule Bioanalysis
- Translational medicine
- Project and data management
- Sample and Labkit management
- Extended Lab Management
Integrated laboratory solutions for clinical trials
Provide central laboratory data for the clinical research and development as well as NDA of new drugs, covering biomarker discovery, method development and validation, clinical verification and application, etc.






