Cell and Gene Therapy QC & Analytics Market 2026-2034 | Size & Trends

Historic Data: 2021-2024   |   Base Year: 2025   |   Forecast Period: 2026-2034

Coverage: Cell and Gene Therapy Quality Control and Analytics Market covers analysis By Testing Type (Sterility Testing, Identity Testing, Potency Testing, Mycoplasma Testing, Endotoxin Testing, Others); Analytical Method (Flow Cytometry, Polymerase Chain Reaction (PCR)/digital PCR (dPCR), High-Performance Liquid Chromatography (HPLC), Mass Spectrometry, Enzyme-Linked Immunosorbent Assay (ELISA), Others); Application Area (Oncology, Genetic Disorders, Cardiovascular Diseases, Infectious Diseases, Others); End-User (Pharmaceutical & Biotechnology Companies, Contract Development and Manufacturing Organizations (CDMOs), Academic & Research Institutes, Others); and Geography

  • Report Date : Feb 2026
  • Report Code : TIPRE00042196
  • Category : Life Sciences
  • Status : Upcoming
  • Available Report Formats : pdf-format excel-format
  • No. of Pages : 150
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Page Updated: Jan 2026

The global cell and gene therapy quality control and analytics market is estimated to be valued at approximately US$ 1.88 billion in 2025. It is projected to reach around US$ 5.38 billion by 2034, representing a compound annual growth rate (CAGR) of 12.40% during 2026–2034.

Cell and Gene Therapy Quality Control and Analytics Market Analysis

The market for quality control (QC) and analytics in the cell and gene therapy (CGT) space is poised for rapid growth. This expansion is driven by the rising number of CGT approvals, increasingly complex therapy modalities (e.g., CAR-T, gene editing, AAV vectors), and stringent regulatory frameworks demanding thorough testing of identity, purity, potency, and stability. Real-time analytics, AI-powered data interpretation, and advanced assay platforms (flow cytometry, PCR/dPCR, mass spectrometry) are increasingly adopted to manage this complexity.

The growth is also fuelled by the outsourcing of QC/analytics services to contract development and manufacturing organizations (CDMOs) and specialized testing labs, as biopharma players focus on core therapy development. The shift from R&D to commercial-scale manufacture intensifies demand for scalable QC analytics infrastructure.

Cell and Gene Therapy Quality Control and Analytics Market Overview

QC and analytics in the CGT domain refer to the suite of processes, technologies, and services used to ensure that cell- and gene-based therapeutic products meet required quality specifications before administration to patients. These include sterility, identity, and potency assays, vector copy number analysis, multi-parameter flow cytometry, immunophenotyping, residual impurity testing, and stability monitoring. QC & analytics systems enable faster batch release, improved manufacturing yield, regulatory compliance, and superior patient safety.
 These solutions are integral to CGT workflows, supporting clinical trial progression, commercial manufacturing, and lifecycle management of advanced therapies.

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Cell and Gene Therapy Quality Control and Analytics Market: Strategic Insights

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Cell and Gene Therapy Quality Control and Analytics Market Drivers and Opportunities

Market Drivers:

  • Rising volume of cell and gene therapy approvals and pipelines: More advanced therapies mean higher demand for sophisticated QC & analytics platforms.
     
  • Stringent regulatory demands for safety, potency, and comparability of CGT products: QC & analytics become a mandatory tool for market entry and post-approval monitoring.
     
  • Increasing outsourcing to specialized labs/CDMOs: As developers scale, QC/analytics services are often externalized, fuelling service-segment growth.
     

Market Opportunities:

  • Integration of AI/ML for predictive analytics and real-time monitoring: Enables smarter analytics and faster batch release decisions.
     
  • Expansion in emerging markets with growing CGT manufacturing footprints (e.g., China, India): Cost-effective analytics platforms and cloud-based solutions will gain traction.
     
  • Development of novel assay platforms (single-cell analysis, multi-omics, digital PCR) tailored for complex CGT products: Offers high-value differentiation for providers.
     

Cell and Gene Therapy Quality Control and Analytics Market Report Segmentation Analysis

By Testing Type:

  • Sterility Testing
  • Identity Testing
  • Potency Testing
  • Mycoplasma Testing
  • Endotoxin Testing
  • Others

By Analytical Method:

  • Flow Cytometry
  • Polymerase Chain Reaction (PCR) / digital PCR (dPCR)
  • High-Performance Liquid Chromatography (HPLC)
  • Mass Spectrometry
  • Enzyme-Linked Immunosorbent Assay (ELISA)
  • Others

By Application Area:

  • Oncology
  • Genetic Disorders
  • Cardiovascular Diseases
  • Infectious Diseases
  • Others

By End-User:

  • Pharmaceutical & Biotechnology Companies
  • Contract Development and Manufacturing Organizations (CDMOs)
  • Academic & Research Institutes
  • Others

By Geography:

  • North America
  • Europe
  • Asia Pacific
  • South & Central America
  • Middle East & Africa

Cell and Gene Therapy Quality Control and Analytics Market Regional Insights

The regional trends and factors influencing the Cell and Gene Therapy Quality Control and Analytics Market throughout the forecast period have been thoroughly explained by the analysts at The Insight Partners. This section also discusses Cell and Gene Therapy Quality Control and Analytics Market segments and geography across North America, Europe, Asia Pacific, Middle East and Africa, and South and Central America.

Cell and Gene Therapy Quality Control and Analytics Market Report Scope

Report Attribute Details
Market size in 2025 US$ 1.88 Billion
Market Size by 2034 US$ 5.38 Billion
Global CAGR (2026 - 2034) 12.40%
Historical Data 2021-2024
Forecast period 2026-2034
Segments Covered By Testing Type
  • Sterility Testing
  • Identity Testing
  • Potency Testing
  • Mycoplasma Testing
  • Endotoxin Testing
  • Others
By Analytical Method
  • Flow Cytometry
  • Polymerase Chain Reaction
By Application Area
  • Oncology
  • Genetic Disorders
  • Cardiovascular Diseases
  • Infectious Diseases
  • Others
By End-User
  • Pharmaceutical & Biotechnology Companies
  • Contract Development and Manufacturing Organizations
Regions and Countries Covered North America
  • US
  • Canada
  • Mexico
Europe
  • UK
  • Germany
  • France
  • Russia
  • Italy
  • Rest of Europe
Asia-Pacific
  • China
  • India
  • Japan
  • Australia
  • Rest of Asia-Pacific
South and Central America
  • Brazil
  • Argentina
  • Rest of South and Central America
Middle East and Africa
  • South Africa
  • Saudi Arabia
  • UAE
  • Rest of Middle East and Africa
Market leaders and key company profiles
  • Thermo Fisher Scientific Inc.
  • Merck KGaA
  • Sartorius AG
  • Danaher Corporation
  • Eurofins Scientific
  • Charles River Laboratories International, Inc.
  • Labcorp Drug Development
  • Catalent, Inc.
  • Bio?Rad Laboratories, Inc.
  • WuXi AppTec

Cell and Gene Therapy Quality Control and Analytics Market Players Density: Understanding Its Impact on Business Dynamics

The Cell and Gene Therapy Quality Control and Analytics Market is growing rapidly, driven by increasing end-user demand due to factors such as evolving consumer preferences, technological advancements, and greater awareness of the product's benefits. As demand rises, businesses are expanding their offerings, innovating to meet consumer needs, and capitalizing on emerging trends, which further fuels market growth.


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Cell and Gene Therapy Quality Control and Analytics Market Share Analysis by Geography

North America

  • Market Share: Holds the largest share globally, driven by advanced CGT infrastructure and regulatory maturity.
  • Key Drivers: Strong R&D investment, large number of CGT approvals, well-established CDMO/QC service providers.
  • Trends: Increased adoption of integrated analytics platforms, cloud-based QC solutions, and real-time batch release testing.

Europe

  • Market Share: Significant share owing to strong regulatory frameworks and public-private initiatives in cell and gene therapies.
  • Key Drivers: EU-wide harmonization of advanced therapy medicinal product regulation (ATMP), rising demand in clinical trials.
  • Trends: Growing interoperability of analytics systems, pan-European QC service networks, and focus on cross-border manufacturing compliance.

Asia Pacific

  • Market Share: Fastest-growing region during the forecast period.
  • Key Drivers: Rapid healthcare and biotech infrastructure expansion, growing CGT manufacturing hubs, and supportive government initiatives.
  • Trends: Adoption of cost-effective cloud-based QC/analytics, localization of service providers, and regional partnerships with global CDMOs.
  1. South & Central America
  • Market Share: Emerging contributor with growth potential.
  • Key Drivers: Expansion of biotech/CGT manufacturing, increasing outsourcing of analytics services to cost-advantage regions.
  • Trends: Cloud-based QC services, regional collaborations, and regulatory enhancements to support advanced therapies.

Middle East & Africa

  • Market Share: Developing but high-potential region.
  • Key Drivers: National e-health and biotech strategies, investments in advanced manufacturing infrastructure.
  • Trends: Adoption of cloud & analytics platforms, growing need for QC/analytics in regional CGT initiatives, partnership models with global providers.

Cell and Gene Therapy Quality Control and Analytics Market Players Density: Understanding Its Impact on Business Dynamics

The QC & analytics market for cell and gene therapies is becoming increasingly competitive due to the presence of global analytics service providers, CDMOs with in-house QC capabilities, and niche analytics platform specialists. This competition drives differentiation through:

  • Seamless integration of analytics and QC platforms with CGT manufacturing workflows.
     
  • Scalable cloud-based QC/analytics solutions tailored for small & large therapy developers.
     
  • AI-enabled automation for assay interpretation, batch release decisions, and trend monitoring.
     
  • Interoperability with manufacturing, CRO, CDMO, and regulatory systems (e.g., LIMS, ELN, regulatory submission platforms).

Opportunities and Strategic Moves:

  • Form alliances with CGT developers and CDMOs to provide comprehensive QC & analytics packages.
     
  • Embed AI/ML and automation into QC workflows for faster turnaround and cost-efficiency.
     
  • Expand presence in emerging markets (Asia-Pacific, Latin America) with regional analytics hubs.
     
  • Invest in next-generation assay platforms (e.g., single-cell sequencing, multi-omics) to stay ahead of the competition.

Major Companies operating in the Cell and Gene Therapy Quality Control and Analytics Market

  1. Thermo Fisher Scientific Inc.
  2. Merck KGaA
  3. Sartorius AG
  4. Danaher Corporation
  5. Eurofins Scientific
  6. Charles River Laboratories International, Inc.
  7. Labcorp Drug Development
  8. Catalent, Inc.
  9. Bio‑Rad Laboratories, Inc.
  10. WuXi AppTec

Other companies analysed during the course of research:

  1. AGC Biologics
  2. Pharmalex
  3. Medpace, Inc.
  4. MilliporeSigma
  5. QIAGEN N.V.
  6. BioReliance

Cell and Gene Therapy Quality Control and Analytics Market News and Recent Developments

  • In April 2025, AGC Biologics launched its dedicated Cell & Gene Technologies Division aimed at supporting developers with enhanced QC & analytics capabilities for advanced therapies.
     
  • Growing use of AI‐driven robotics platforms in CGT manufacturing and QC; for example, a collaboration in 2025 validated a fully automated cell therapy production and QC platform, enabling decentralized manufacturing.
     
  • Biopharma and CDMO investment in regional analytics hubs is increasing to meet cost and regulatory pressures, particularly in the Asia-Pacific.
     
  • Rising regulatory scrutiny of CGT products requiring advanced analytics (single-cell, multi-omics) and real‐time release testing is driving service demand.
     

Cell and Gene Therapy Quality Control and Analytics Market Report Coverage and Deliverables

The "Cell and Gene Therapy Quality Control and Analytics Market Size and Forecast (2024–2034)" report provides a detailed analysis covering the following:

  • Market size and forecast at global, regional, and country levels for all key market segments covered under the scope
     
  • Market trends, including market dynamics such as drivers, restraints, and key opportunities
     
  • Detailed PEST and SWOT analysis
     
  • Market analysis covering key market trends, global and regional frameworks, major players, regulations, and recent market developments
     
  • Industry landscape and competition analysis covering market concentration, heat-map analysis, prominent players, and recent developments in the QC & analytics segment of the CGT market
     
  • Detailed company profiles

Frequently Asked Questions

1

What are the key drivers of market growth?

1. Rising approvals and pipelines of cell and gene therapies.
2. Increasing regulatory stringency on QC, potency, and analytics for advanced therapies.
3. Growing outsourcing of QC/analytics to CDMOs and specialist labs.
2

Which component or segment is gaining traction?

The analytical methods segment (e.g., PCR/dPCR, mass spectrometry, flow cytometry) and the services segment (outsourced analytics) are gaining traction, driven by complex therapy modalities and the need for advanced characterization.
3

Which industries are the primary end-users of QC & analytics in CGT?

1. Pharmaceutical & biotechnology companies developing cell & gene therapies.
2. Contract development and manufacturing organizations (CDMOs) offering QC/analytics support.
3. Academic & research institutes involved in translational CGT work.
4

What are some of the leading companies in the market?

Major players include Thermo Fisher Scientific, Merck KGaA, Sartorius, Danaher, Eurofins Scientific, Charles River Laboratories, Catalent, Bio-Rad, Labcorp Drug Development, and WuXi AppTec.
5

Which challenges hinder market growth?

Key challenges include high cost and complexity of analytics platforms, the requirement for highly skilled talent, and regulatory variability across geographies affecting global scalability.
Mrinal Kerhalkar
Manager,
Market Research & Consulting

Mrinal is a seasoned research analyst with over 8 years of experience in Life Sciences Market Intelligence and Consulting. With a strategic mindset and unwavering commitment to excellence, she has built deep expertise in pharmaceutical forecasting, market opportunity assessment, and developing industry benchmarks. Her work is anchored in delivering actionable insights that empower clients to make informed strategic decisions.

Mrinal’s core strength lies in translating complex quantitative datasets into meaningful business intelligence. Her analytical acumen is instrumental in shaping go-to-market (GTM) strategies and uncovering growth opportunities across the pharmaceutical and medical device sectors. As a trusted consultant, she consistently focuses on streamlining workflow processes and establishing best practices, thereby driving innovation and operational efficiency for her clients.

  • Historical Analysis (2 Years), Base Year, Forecast (7 Years) with CAGR
  • PEST and SWOT Analysis
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