Towards Healthcare Research & Consulting

Everything You Need to Track the Global Cell & Gene Therapy Ecosystem - All in One Dashboard

Explore Dashboard

1300+

Pipeline Programs

900+

CGT Companies Tracked

500+

Manufacturing Facilities

Cell Therapy Human Raw Materials Market Demand, Size and Growth Rate Forecast 2035

According to Payal Rabde, who specializes in blood-derived products, tissues, primary cells, growth factors, and other biological materials used in cell therapy, research development, and manufacturing, with 4+ years of experience in market research and industry analysis, extensive research indicates strong growth opportunities in the cell therapy human raw materials market. The global cell therapy human raw materials market size was estimated at USD 4.35 billion in 2025 and is predicted to increase from USD 5.32 billion in 2026 to approximately USD 22.75 billion by 2034, expanding at a CAGR of 22.38% from 2025 to 2034. The market is expanding due to rising cell therapy development, increasing demand for high-quality biological materials, growing clinical research, and advances in regenerative medicine.

Last Updated : 26 August 2026 Insight Code: 5207 Format: PDF / PPT / Excel ✓ Fact Checked ❝ Cite Cell Therapy Human Raw Materials Market Increases 22.38% CAGR by 2034
Source: https://www.towardshealthcare.com/insights/cell-therapy-human-raw-materials-market-sizing
Revenue, 2025
USD 4.35 Billion
Forecast, 2035
USD 22.75 Billion
CAGR, 2026-2035
22.38%
Report Coverage
Global

The global cell therapy human raw materials market size was estimated at US$ 4.35 billion in 2025 and is projected to grow to US$ 22.75 billion by 2034, rising at a compound annual growth rate (CAGR) of 22.38% from 2023 to 2034.

Cell Therapy Human Raw Materials Market Revenue 2023 - 2034

Key Takeaways

  • Cell therapy human raw materials sector push the market to USD 5.32 billion by 2026
  • Long-term projections show USD 22.75 billion valuation by 2034
  • Growth is expected at a steady CAGR of 22.38% in between 2025 to 2034
  • By region, North America dominated the market share by 45.80% in 2025.
  • By region, Asia Pacific is expected to grow at the fastest rate during the forecast period.
  • By product, the cell culture supplements segment held the largest share of the cell therapy human raw materials market in 2025.
  • By product, the cell culture media segment is anticipated to grow at the fastest rate during the forecast period.
  • By end-use, the biopharmaceutical & pharmaceutical companies segment dominated the market in 2025.
  • By end-use, the CROs & CMOs segment is expected to showcase the fastest CAGR during the predicted period.

Cell Therapy Human Raw Materials Market: Therapeutics

Cell therapy has become a very exciting area of study with novel therapeutic possibilities for a variety of illnesses. Although human cells are essential components for producing products for cell therapy, they frequently bring about a great deal of variability. On the other hand, the optimal collection of high-quality, consistent cellular material is made possible by strict operational controls and quality systems. The functioning of raw materials employed in cell therapy must enable desirable cellular activity. This covers the survival, differentiation, and multiplication of cells. It is crucial to choose raw materials that are suitable for the targeted therapeutic applications and the particular cell types.

How can AI Improve Cell Therapy Human Raw Materials Market?

The immense potential of artificial intelligence in healthcare is demonstrated by the industry's rapid expansion and large investments in R&D. The industrial industry is expected to face a financial effect of $3.8 trillion by 2035, while the AI market is predicted to reach an astounding $407 billion by 2027. The healthcare sector has been the most heavily invested in, with an estimated $6.1 billion in 2022. Over the past ten years, artificial intelligence (AI) and machine learning (ML) predictive techniques have transformed various biological domains, such as genome annotation, protein structure prediction, and synthetic enzyme design. By applying these predictive techniques to the creation of cell treatments, it may be possible to create better cell therapies more quickly and with fewer resources.

For instance,

  • In January 2024, CellVoyant, founded by a biotechnology business with a background in artificial intelligence (AI) and spun out of the University of Bristol, secured £7.6 million in seed money to further the development of innovative cell treatments. As per the news statement dated January 16, 2024, Octopus Ventures spearheaded the investment round, which also involved participation from Horizon Ventures, Verve Ventures, and Air Street Capital.

Market Data & Statistics

  • The U.S. Food and Drug Administration (FDA) approved a total of 43 cell and gene therapy products as of January 2025.
  • The American Cancer Society estimates more than 2 million new cancer cases and more than 0.6 million cancer-related deaths in 2025.
  • As of May 14, 2025, there are around 5,825 recruiting and active, not recruiting clinical trials registered on the clinicaltrials.gov website related to cell therapy as an intervention.

Strategic Initiatives

  • In March 2023, the World Health Organization (WHO) Expert Committee on Biological Standardization adopted its first guidance document for cell, tissue, and gene therapy products. The document encourages all countries to establish a regulatory framework for such products and implement the concepts of regulatory cooperation, harmonization, and reliance.
  • The Centers for Medicare and Medicaid Services (CMS), by the U.S. government, launched the “Cell and Gene Therapy (CGT) Access Model” to increase the access of these products to people with Medicaid living with rare and severe diseases.
  • The Chinese government's stem cell initiatives focus on funding and regulatory frameworks designed to encourage scientific advancement and innovation. The National Health Commission of China allocated more than 5 billion RMB ($765 million) to stem cell research projects as of 2023.
  • The UK National Health System (NHS) formed the SAMPLE Program, a Standard Approach to ATMP Tissue Collection, to expand the use of next-generation cell and gene therapies for cancer and non-cancer illnesses in the UK.

Cell Therapy Human Raw Materials: Fueling the Future of Advanced Therapies

Cell therapy human raw materials are biological and specialized ingredients used in the development and manufacturing of cell-based therapies, including culture media, growth factors, cytokines, supplements, and other essential components. The market is expanding due to the growing development of cell-based treatments and increasing investments in advanced therapeutic research. Current trends include demand for GMP-grade, xeno-free, serum-free, and chemically defined materials to improve safety and manufacturing consistency.

Technological advancements in gene editing, automated cell processing, cryopreservation, and closed-system manufacturing are creating demand for more specialized raw materials. Key drivers include increasing clinical trials, expansion of biopharmaceutical manufacturing, and growing interest in personalized medicines. Future opportunities are emerging in CAR-T therapies, stem cell treatment, NK-cell therapies, and iPSC-based applications, supporting demand for reliable, scalable, and high-quality raw material solutions.

Market Dynamics

Personalized Medicine Drives the Market

The cell therapy human raw materials market is growing due to the growing demand for personalized medicines due to various genetic, autoimmune, and chronic conditions along with cancer. These diseases require personalized medicines for better quality of care and better health outcomes. During cell therapy, the genetic material of an individual is used along with environmental conditions and lifestyle to develop better cell therapies, which will require human raw materials from individuals for testing and other purposes.

Market Restraint: Risk of Contamination and Variability

One of the biggest obstacles is the inherent danger of contamination and unpredictability in human raw ingredients. Striving for repeatability in cell treatments requires maintaining consistency in cell quality and features. Therefore, possible obstacles such as contamination and variability exist.

Opportunity: Expansion of Cell Sources

Further investigation into other cell sources, such as hematopoietic stem cells (HSCs), induced pluripotent stem cells (iPSCs), and mesenchymal stem cells (MSCs), among others, offers a chance to grow the industry. Cell treatments may be made more versatile and applicable by investigating and adding novel cell types.

There are currently close to 400 million rare illness patients globally as the frequency of these conditions rises yearly. Certain malignancies and uncommon disorders may be treated or even cured with cell and gene therapy (CGT). There may soon be a surge of novel gene treatments available. Over the next five years, it is anticipated that the CGT will almost triple. The numerous qualities of cell/gene therapy make it a wise option for treating uncommon ailments. Once mastered, replacing or repairing damaged genes is a highly reproducible strategy that may be used to treat a wide range of genetic illnesses.

For instance,

  • In July 2024, the US Food and Drug Administration (FDA) established a new rare illness innovation hub with the goal of accelerating the development and approval of orphan medications. Clinical trials for rare diseases can be challenging to understand, particularly for disorders with small patient populations. Furthermore, because of the high development costs, certain rare illness medicines have been abandoned by businesses even after they have shown clinical effectiveness.

Market Segmentations

By Product Insights

Why Did the Cell Culture Supplements Segment Dominate in the Market?

By product, the cell culture supplements segment held the largest share of the cell therapy human raw materials market in 2025. With the use of cell culture supplements, labs can modify and enhance media formulations to meet the needs of certain cell culture applications, including the creation of proteins, hybridomas, Chinese hamster ovary (CHO) cells, various serum-free processes, and more. The supplements evaluated in cell culture and insect culture that are gathered here have been applied and tested to ensure that they work well in cell culture systems. Many culture parameters, including the right medium composition for your cell line, are critical to ensuring proper cell development. Basal or complex media can be improved and supplemented with lipids, vitamins, amino acids, serum, and antibiotics to assist cell development.

For instance,

  • In July 2024, precision stem cell cultivation has new options thanks to the partnership between Qkine and StemCultures. The biosciences business StemCultures, which is committed to creating novel reagents that improve the quality and efficiency of cell growth and differentiation in culture, has formed a new cooperation with Qkine, a maker of specialized bioactive proteins.
  • In May 2023, a performance-enhancing peptide for cell culture medium used in the production of biological medicines, cQrex® KC, will be available from Evonik. The biopharmaceutical industry's media formulators and cell culture process developers may now optimize cystine supply and boost cell culture productivity thanks to this novel peptide.

The Cell Culture Media Segment: Fastest-Growing

By product, the cell culture media segment is anticipated to grow at the fastest rate in the cell therapy human raw materials market during the forecast period. For the purpose of supplying the elements required to sustain cell growth and function, cell culture media is essential. The nutrients and growth factors your culture environment needs for the cells to behave as predicted are provided by components in the cell culture medium. Furthermore, media may be designed to control pH and osmotic pressure, two other environmental factors in cell growth. Different formulations of cell culture medium have been created to accommodate a broad range of cell types and experimental uses.

For instance,

  • In July 2023, the life science division of Merck KGaA, Darmstadt, Germany, stated that MilliporeSigma, its U.S. and Canadian subsidiary, has expanded its Lenexa, Kansas, location by adding 98,000 square feet of lab space and manufacturing capacity for cell culture medium.

By End-Use Insights

What Made Biopharmaceutical & Pharmaceutical Companies the Dominant Segment in the Market?

By end-use, the biopharmaceutical & pharmaceutical companies segment dominated the cell therapy human raw materials market in 2025. Cell and gene therapy is being used by pharmaceutical corporations to treat complicated medical diseases and expand treatment alternatives. Pharmaceutical corporations are strategically investing in cell and gene therapy in addition to concentrating on innovation to expand their patent portfolios. The goal of these expenditures is to put oneself at the forefront of industry innovations and close profitable partnerships with partners. A few of the most recent agreements highlight the significance of gene and cell therapy for the pharmaceutical sector.

The CROs & CMOs Segment is the Fastest Growing

By end-use, the CROs & CMOs segment is expected to showcase the fastest CAGR in the cell therapy human raw materials market during the predicted period. Biotechnology and pharmaceutical businesses frequently turn to third-party suppliers for development and manufacturing help, most frequently to CROs, CMOs, or CDMOs, in order to manage industry challenges and fill resource shortfalls. Both bio/pharma businesses and CDMOs continue to invest in the development and manufacturing capabilities for cell and gene treatments, which represent a niche but expanding industry on a product basis. Due to the industry's limited capacity for these novel modalities, CDMOs of all sizes continue to make investments in research and development as well as production capacity.

Regional Analysis

Multiple Factors Promote North America’s Dominance

By region, North America dominated the cell therapy human raw materials market share by 45.80% in 2025. The region's dominance may be attributed to supportive government policies, an increasing need for innovative treatments, and coordinated efforts by significant industry players to improve cell therapy products that treat a range of chronic illnesses. Furthermore, North America is home to a large number of well-known businesses that produce and sell cell-based goods, which is driving up demand for human raw materials for cell therapy and further expanding the market. Moreover, joint ventures between major industry participants and smaller biotechnology enterprises intensify rivalry as firms endeavor to strengthen their positions in the constantly changing cell therapy sector.

For instance,

  • In May 2024, regarding the use of materials and components derived from humans and animals in the production of tissue-engineered medical products and cell and gene therapy, the FDA released a new draft of guidance for public comment. In April 2024, the FDA's Center for Biologics Evaluation and Research released the draft paper. A set of guidelines for guaranteeing the safety, identity, and quality of materials (of both human and animal origin) used in the production of tissue-engineered medical products (TEMPs) and cellular and gene therapy (CGT) products is included in the draft guidance.

U.S. Market Trends

The presence of well-developed R&D infrastructures in the U.S. is increasing the demand for cell therapy raw materials due to growing innovations in CAR-T, personalized, and stem cell therapies. The stringent regulations and growth in healthcare investments are also increasing their demand.

Canada: Emerging Hub for Cell Therapy Raw Materials

Canada’s cell therapy raw materials market is growing due to increasing investment in biotechnology, expanding cell and gene therapy research, and strengthening biomanufacturing infrastructure. Government initiatives and collaboration between research institutions and industry are supporting innovation in advanced therapies. Rising demand for high-quality standardized and GMP-grade raw materials, along with growing clinical development activities, is further creating opportunities for market expansion.

Cell Therapy Demand Drives Asia Pacific’s Market

By region, Asia Pacific is expected to grow at the fastest rate during the forecast period. The rise in demand for advanced cell treatments and the heightened emphasis on biotechnology are the reasons for this surge. The market is growing because of the establishment of manufacturing facilities, strategic partnerships, and increased R&D activity by major industry players. Additionally, the Asia-Pacific region's highest market share belonged to China's Cell Therapy Human Raw Materials market, while India's Cell Therapy Human Raw Materials market grew at the quickest rate.

CAR-T Cell Therapies Approved in Asia
Brand Manufacturer Country Year of Approval
Carvykti Legend Biotech, J&J Japan & South Korea 2023
Yuanruida (CNCT19) JUVENTAS China 2023
Carteyva JW Therapeutics China 2021
Fucaso IASO BIO, Innovent China 2023
Saikaize (Zevor-cel) Carsgen Therapeutics China 2024
Abecma BMS, bluebird bio Japan 2022
Breyanzi BMS Japan 2021
Yescarta Kite Pharma, Fosun Kite Japan & China 2021
Kymriah Novartis Japan, South Korea and Taiwan 2021

China Market Trends

The expanding industries in China are increasing the development of regenerative and cell & gene therapies, which is driving the demand for cell therapy raw materials. At the same time, the growing government initiatives, increasing disease burden, and expanding development of generic products are also increasing their use.

India Emerges as a growth engine for Cell Therapy Raw Materials

India is notably expanding in the cell therapy human raw materials market due to rising biotechnology research, increasing cell and gene therapy development, and growing healthcare innovation. The country’s expanding biopharmaceutical manufacturing base, skilled workforce, and cost-effective research capabilities are attracting greater investment. Growing clinical studies and demand for specialized culture media, growth factors, reagents, and other essential inputs are further supporting market development.

Stringent Regulations Boost Europe

Europe is expected to grow significantly in the cell therapy raw materials market during the forecast period, due to a robust regulatory framework, which increases the use of high-quality raw materials for cell therapies. The growing gene therapy clinical pipeline is also increasing their demand, where the growing R&D activities and their increasing adoption rates are also enhancing the market growth.

UK Market Trends

The growing advancements in cell and gene therapies in the UK are increasing the demand for their raw materials. The growing adoption of cell therapies and regenerative medicines is also increasing their use, where the growing demand for personalized medicine and stringent regulations are also promoting their use.

Germany Strengthened Cell Therapy Raw Materials Growth

Germany is notably expanding in the cell therapy human raw materials market due to its advanced biotechnology sector, strong research capabilities, and increasing development of cell and gene therapies. Growing biopharmaceutical manufacturing activities are driving demand for specialized raw materials. The country’s skilled workforce, established scientific infrastructure, and increasing focus on innovative therapeutic solutions are further supporting market growth.

Market Value Chain Analysis

R&D

  • The R&D of the cell therapy raw materials focuses on engineering chemically defined, high-purity cytokines and animal-free media.
  • Key players: Thermo Fisher Scientific, Merck KGaA, Sartorius.

Clinical Trials and Regulatory Approvals

  • The sterility, absence of adventitious agents, compendial compliances, certificate of analysis (CoA), and drug master files (DMF) are evaluated in the clinical trials and regulatory approvals of the cell therapy raw materials.
  • Key players: Thermo Fisher Scientific, Merck KGaA, Sartorius.

Formulation and Final Dosage Preparation

  • The formulation and final dosage preparation of the cell therapy raw materials involves the use of automated closed system technologies to integrate specialized cryoprotectant and sterile fill-finish process, ensuring cell viability and potency in the final dosage form.
  • Key players: Thermo Fisher Scientific, Lonza, Catalent.

Patient Support and Services

  • Regulatory consulting services and ancillary material qualification are provided in the patient support and services of the cell therapy raw materials.
  • Key players: Thermo Fisher Scientific, Merck KGaA, Sartorius.

Top Companies in the Cell Therapy Human Raw Materials Market

  • Thermo Fisher Scientific, Inc
  • REPROCELL
  • Actylis
  • STEMCELL Technologies
  • ACROBiosystems
  • Charles River Laboratories
  • BioIVT
  • PromoCell GMBH
  • Pluri Inc.
  • AllCells
  • GeminiBio
  • Akron Biotech
  • Danaher
  • RoosterBio, Inc.
  • Grifols, S.A.
  • Merck KGaA
  • CGT Global

Innovation by REPROCELL in the Cell Therapy Human Raw Materials Market

Company Name REPROCELL
Headquarters Kanagawa, Japan, Asia Pacific
Recent Development In May 2024, REPROCELL generated human-induced pluripotent stem cells (hiPSCs) that were therapeutically relevant by managing the donor recruiting process for seed stock hiPSCs and ensuring donor eligibility with several regional regulatory bodies. Strict selection is applied to the raw materials, and a patented technique for footprint-free RNA reprogramming is employed. In order to produce hiPSC and hMSC that are appropriate for therapeutic application, REPROCELL has recently expanded this offering by purchasing a Cytocentric Xvivo system model 2 from BioSpherix, which is a closed GMP cell culturing system.

Innovation by Pluri Inc. in the Cell Therapy Human Raw Materials Market

Company Name Pluri Inc.
Headquarters Haifa, Israel, Middle East
Recent Development In January 2024, the biotech company Pluri Inc. introduced PluriCDMO, a new business division that provides contract development and manufacturing organization (CDMO) services for cell therapy production. From its cutting-edge, 47,000-square-foot GMP cell therapy production facility, PluriCDMO will provide development and manufacturing services to assist clients in overcoming significant obstacles in the creation and manufacture of cell-based medicines.

Latest Announcements by Industry Leaders

  • In May 2026, "Made Scientific has demonstrated a clear commitment to manufacturing excellence and a genuine understanding of what it takes to bring cell therapies from development into commercial reality," "Integrating our MSC and EV manufacturing platforms into Made Scientific's CDMO infrastructure gives advanced therapy developers access to a proven, scalable manufacturing platform and accelerates the path to commercially viable MSC-based therapeutics”, said Tim Kelly, CEO of RoosterBio.

Segments Covered in the Report

By Product

  • Cell Culture Supplements
    • Proteins
    • Growth Factors
    • Nucleotides
    • Other Supplements
  • Cell Culture Media
  • Cell Culture Sera
  • Reagents & Buffers
  • Other Raw Materials

By End-Use

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

By Region

  • North America
    • U.S.
    • Canada
  • Asia Pacific
    • China
    • Japan
    • India
    • South Korea
    • Thailands
  • Europe
    • Germany
    • UK
    • France
    • Italy
    • Spain
    • Sweden
    • Denmark
    • Norway
  • Latin America
    • Brazil
    • Mexico
    • Argentina
  • Middle East and Africa (MEA)
    • South Africa
    • UAE
    • Saudi Arabia
    • Kuwait

FAQ's

Finding : Cell treatments have the potential to cure a variety of conditions, such as cancer, autoimmune diseases, infections, urinary tract issues, and spinal cord injuries. They may also aid patients with neurological disorders and replace damaged joint cartilage.

Finding : The whole dosage falls between 3 × 106 and 3 × 107 cells/kg. Administered in increasing dosages, with the goal doses of 109 or 1010 cells being reached after starting at 106 cells.

Finding : National Institutes of Health, FDA, WHO, Centers for Disease Control and Prevention, Department of Biotechnology.

Meet the Team

Payal Rabde

Payal Rabde

Principal Consultant

Payal Rabde is a Healthcare Market Research Analyst at Towards Healthcare Research & Consulting with 4+ years of experience in pharmaceuticals, biotechnology, medical devices, and life sciences.

Learn more about Payal Rabde
Aditi Shivarkar

Aditi Shivarkar LinkedIn

Reviewed By

Aditi Shivarkar is a seasoned professional with over 14 years of experience in healthcare market research. As a content reviewer, Aditi ensures the quality and accuracy of all market insights and data presented by the research team.

Learn more about Aditi Shivarkar
Cell Therapy Human Raw Materials Market
Updated Date: 26 August 2026   |   Report Code: 5207
Schedule a Meeting next-arrow