Date : 14 October 2025

The global viral vector-based cell & gene therapy CDMO market size is calculated at US$ 142.77 million in 2024, grew to US$ 162 million in 2025, and is projected to reach around US$ 497.7 million by 2034. The market is expanding at a CAGR of 13.44% between 2025 and 2034.
The R&D process in the Viral Vector-Based Cell & Gene Therapy CDMO market includes various stages such as preclinical and early process development, late-stage process development, process validation, and cGMP manufacturing.
Key Players: Lonza, Thermo Fisher Scientific (Patheon), Catalent, FUJIFILM Diosynth Biotechnologies, and Charles River Laboratories.
The clinical trials are driven by outsourcing demand and capacity expansion. The regulatory approvals are given by the USFDA, China's National Medical Products Administration (NMPA), and European EMA.
Key Players: Lonza, Catalent, Thermo Fisher Scientific Inc., Charles River Laboratories, AGC Biologics.
These services include logistics, supply chain management, patient education and engagement, financial and regulatory support.
Key Players: Thermo Fisher Scientific Inc., Lonza, Catalent, Charles River Laboratories, Novartis.
In April 2025, Wolfgang Wienand, Chief Executive Officer of Lonza announced the launch of its new CDMO structure with three business platforms such as integrated biologics, advanced synthesis, and specialized modalities. This innovation brought into practice to enhance customer proximity, strengthen company’s multimodality offering, and provide scalability for future growth.
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