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Advanced therapeutics, such as cell and gene therapies, have the immense potential to revolutionize healthcare. However, the path from translational studies to clinical trials and commercial manufacturing is riddled with challenges and risks. Therefore, it’s essential to partner with a CDMO with the experience, capacity, network, and ability to adapt and personalize its development approach.
With our extensive expertise, end-to-end services, and robust global supply network, we can effectively help biotechnology and pharmaceutical companies navigate the journey from molecule to medicine. Our portfolio of capabilities is equipped to handle your unique needs and empowers you to confidently meet critical timelines and bring your therapy to market, transforming lives worldwide.
This brochure outlines our end-to-end advanced therapy contract development and manufacturing organization (CDMO) services, including:
- Translational research services
- Viral vector development and manufacturing services
- Cell therapy development and manufacturing services
- mRNA development and manufacturing services
- Cold and ultracold clinical supply chain management
- Quick to CareTM advanced therapies program
