PUBLISHER: Bizwit Research & Consulting LLP | PRODUCT CODE: 1799510
PUBLISHER: Bizwit Research & Consulting LLP | PRODUCT CODE: 1799510
The Global Cell & Gene Therapy Manufacturing Services Market, valued at approximately USD 7.04 billion in 2024, is projected to expand at a striking CAGR of 17.50% from 2025 to 2035. As the life sciences sector pushes the boundaries of modern medicine, cell and gene therapy manufacturing services have emerged as a vital bridge between groundbreaking research and large-scale therapeutic delivery. These specialized services encompass a broad spectrum of capabilities-from process development and viral vector production to commercial-scale manufacturing-enabling biopharmaceutical companies to accelerate the translation of advanced therapies into market-ready treatments. Increasing incidences of genetic disorders, a growing pipeline of cell and gene therapy candidates, and regulatory incentives for regenerative medicine are collectively propelling the market forward. Meanwhile, advancements in automation, closed-system manufacturing, and scalable bioprocessing platforms are redefining efficiency, cost-effectiveness, and global accessibility of these life-saving modalities.
The momentum within this market is further amplified by the exponential growth in oncology-focused therapies, with CAR-T and TCR-based treatments leading the charge. These transformative therapies demand highly controlled, GMP-compliant environments and expert handling, pushing pharmaceutical and biotech firms to seek specialized contract development and manufacturing organizations (CDMOs) with deep technical expertise. Moreover, the rise of allogeneic approaches promises to overcome the scalability and cost challenges associated with autologous therapies, broadening patient accessibility. As precision medicine gains wider adoption, demand for flexible manufacturing capacities capable of rapid scale-up for both clinical trials and commercial distribution is soaring. Industry collaborations, multi-site manufacturing footprints, and robust quality management systems are becoming non-negotiable for success in this rapidly evolving landscape.
Regionally, North America is anticipated to command the largest share of the market in 2025, bolstered by its strong biotechnology ecosystem, high concentration of clinical trials, and advanced regulatory frameworks that support expedited approval pathways for regenerative medicines. Europe continues to strengthen its position through substantial investments in manufacturing infrastructure, collaborative R&D networks, and supportive funding programs from the European Medicines Agency and national governments. Meanwhile, Asia Pacific is expected to witness the fastest growth over the forecast period, driven by increasing government investment in biotechnology hubs, the rise of contract manufacturing in countries like China, South Korea, and Singapore, and an expanding patient pool for genetic and oncology disorders. The region's growing capabilities in cost-efficient manufacturing, coupled with favorable regulatory reforms, are attracting global players to establish production partnerships and innovation centers in the region.
The objective of the study is to define market sizes of different segments & countries in recent years and to forecast the values for the coming years. The report is designed to incorporate both qualitative and quantitative aspects of the industry within the countries involved in the study. The report also provides detailed information about crucial aspects, such as driving factors and challenges, which will define the future growth of the market. Additionally, it incorporates potential opportunities in micro-markets for stakeholders to invest, along with a detailed analysis of the competitive landscape and product offerings of key players. The detailed segments and sub-segments of the market are explained below: