Cell Therapy Human Raw Materials Market- Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Product, By End User, By Region & Competition, 2021-2031F

The Global Cell Therapy Human Raw Materials Market is projected to expand from USD 3.01 Billion in 2025 to USD 6.08 Billion by 2031, registering a CAGR of 12.43%. These raw materials encompass biological substances sourced from human donors, including leukopaks and serum albumin, which are indispensable for manufacturing therapeutic products. Key drivers propelling market growth include the increasing global incidence of oncological diseases requiring personalized interventions and heightened capital allocation for regenerative medicine research. This dynamic clinical environment fuels the demand for high-quality biological inputs essential for the development of new immunotherapies.

However, the market encounters significant challenges regarding the strict regulatory compliance needed for sourcing donor-derived materials, often resulting in supply chain complexities. Manufacturers must navigate diverse international standards for donor eligibility and material safety, which can hinder rapid scalability. According to the International Society for Cell & Gene Therapy, the global pipeline included 3,063 therapies in 2024, marking a 7.5% increase from the first half of the year; this volume imposes immense pressure on existing supply networks.

Market Driver

The surge in cell therapy clinical trials and R&D investment serves as a primary catalyst for the raw materials market, creating an urgent need for scalable supply chains. As biopharmaceutical companies and research institutions accelerate their development programs, the demand for high-grade biological inputs like human serum and leukopaks has intensified. This influx of capital allows developers to advance candidates through costly late-stage trials, thereby increasing the volume of raw materials required for process development and manufacturing. According to the Alliance for Regenerative Medicine, the sector attracted $10.9 billion in investment during the first half of the year as of October 2024, providing the necessary liquidity to sustain these resource-intensive phases.

Simultaneously, the expansion of manufacturing capabilities by CDMOs and biopharma companies is directly addressing bottlenecks in raw material availability. To mitigate supply shortages and ensure compliance with Good Manufacturing Practice (GMP) standards, key industry players are investing heavily in infrastructure that supports the production of ancillary materials. This strategic broadening of internal and external capacity ensures that the supply chain can withstand the pressures of commercial-scale production. For instance, BioIVT opened a new cleanroom manufacturing facility in Winchester, Virginia, in August 2024, specifically designed to enhance the output of GMP-compliant ancillary materials. These advancements are critical to supporting the rapidly growing ecosystem; according to the American Society of Gene & Cell Therapy, the global development pipeline comprised over 4,000 gene, cell, and RNA therapies in April 2024.

Market Challenge

The stringent regulatory compliance required for sourcing donor-derived materials acts as a significant restraint on the Global Cell Therapy Human Raw Materials Market. Since these inputs are biological, they are subject to rigorous safety protocols regarding donor eligibility. However, the lack of global harmonization creates a fragmented landscape where material validated for one region may not meet the criteria of another. This discrepancy compels manufacturers to establish segregated supply chains and conduct redundant testing, which directly impedes operational efficiency and slows the commercialization of therapies.

These regulatory hurdles are particularly damaging given the intensification of industry activity, which demands a seamless flow of resources. The inability to easily transfer raw materials across borders restricts the flexibility needed to meet global clinical trial demands. According to the Alliance for Regenerative Medicine, the sector reported a 6% increase in the number of developers globally in 2025. This expansion in companies vying for limited, compliant donor material exacerbates supply shortages, ultimately hampering the overall growth potential of the market.

Market Trends

The increased utilization of characterized leukopaks for allogeneic therapies is fundamentally reshaping the raw materials landscape by prioritizing scalable, donor-derived starting materials over patient-specific sources. As developers shift toward off-the-shelf modalities to reduce manufacturing costs, there is a critical requirement for leukopaks that are GMP-compliant and extensively characterized for specific HLA types to ensure consistency across large batches. This transition necessitates robust donor networks and high-throughput processing capabilities to maintain a steady supply of high-quality cellular starting material. According to BioLife Solutions, in their 'Third Quarter 2024 Financial Results' released in November 2024, the company reported a 43% increase in cell processing platform revenue compared to the prior year, highlighting the surging industrial demand for validated biopreservation and starting material solutions.

The widespread adoption of Human Platelet Lysate (HPL) as a xeno-free supplement is accelerating as manufacturers seek to eliminate the safety risks associated with animal-derived components like Fetal Bovine Serum. This trend is driven by the need for chemically defined, pathogen-reduced media that supports the clinical-grade expansion of Mesenchymal Stem Cells and T-cells without compromising phenotypic stability. Consequently, suppliers are expanding their manufacturing infrastructure to provide standardized, viral-inactivated HPL formulations that meet stringent international quality standards. According to PL BioScience, in the August 2024 press release 'PL BioScience closes Series A Financing', the company secured €7.8 million specifically to scale up its production capacities, reflecting the sector's urgent move toward sustainable, non-animal derived culture systems.

Key Market Players

• Thermo Fisher Scientific, Inc.
• Merck KgaA
• Danaher Corporation
• Sartorius AG
• Aceto Holding GmbH
• Acrobiosystems Inc.
• Grifols, S.A
• Charles River Laboratories International, Inc.
• RoosterBio, Inc

Report Scope

In this report, the Global Cell Therapy Human Raw Materials Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:

Cell Therapy Human Raw Materials Market, By Product

• Cell Culture Media
• Cell Culture Sera
• Cell Culture Supplements
• Reagents & Buffers
• Other

Cell Therapy Human Raw Materials Market, By End User

• Biopharmaceutical & Pharmaceutical Companies
• CROs & CMOs
• Academic & Research Institutions

Cell Therapy Human Raw Materials Market, By Region

• North America
  • United States
  • Canada
  • Mexico
• Europe
  • France
  • United Kingdom
  • Italy
  • Germany
  • Spain
• Asia Pacific
  • China
  • India
  • Japan
  • Australia
  • South Korea
• South America
  • Brazil
  • Argentina
  • Colombia
• Middle East & Africa
  • South Africa
  • Saudi Arabia
  • UAE

Competitive Landscape

Company Profiles: Detailed analysis of the major companies present in the Global Cell Therapy Human Raw Materials Market.

Available Customizations:

Global Cell Therapy Human Raw Materials Market report with the given market data, TechSci Research offers customizations according to a company's specific needs. The following customization options are available for the report:

Company Information

• Detailed analysis and profiling of additional market players (up to five).