Clionix provides Contract Development and Manufacturing Organization (CDMO) services designed to support partners across the full lifecycle of radiopharmaceutical product development and production.
We establish and manage CDMO infrastructures in the regions where you need them — offering end-to-end capabilities that cover early-stage clinical research through to full-scale commercial manufacturing.
Our approach combines technical excellence, regulatory compliance, and operational flexibility, ensuring your products are developed and manufactured efficiently, safely, and to the highest global standards.
| Service Area | Details |
|---|---|
| Infrastructure Establishment | Setup and operation of CDMO facilities in desired geographies |
| Process Development | Optimization of synthesis and labeling processes for radiopharmaceuticals |
| Analytical & Quality Control Support | Development of QC methods, validation, and release testing |
| Clinical Supply Manufacturing | GMP-compliant production of batches for clinical trials |
| Commercial Manufacturing | Scalable production for approved radiopharmaceutical products |
| Regulatory & Documentation Support | Preparation of GMP and ICH-aligned technical documentation |
| Technology Transfer & Validation | Transfer of existing technologies into new CDMO environments |
| Supply Chain & Logistics | End-to-end coordination of material supply, transport, and regulatory distribution |