Cell and Gene Therapy Manufacturing Services Market
Report Scope:
The scope of this study encompasses an investigation of cell and gene therapy manufacturing services. BCC Research analyzes the manufacturing services based on therapy type, application, disease, and end user. BCC determines the current market status in each segment, examines its impact on future markets, and presents growth forecasts over the next six years. The recent report provides a detailed analysis of the market's drivers, challenges, and opportunities. The report also covers market projections to 2028 and market share for key market players. The report includes the company profiles of the key players with detailed information about their business segments, financials, product portfolios, and recent developments. The report also provides the ESG perspective, emerging technologies, and investment outlook.
Report Includes:
34 data tables and 18 additional tables
An overview of the global cell and gene therapy manufacturing services market
Analyses of global market trends, with data from 2020-2022, estimates for 2023, and projections of compound annual growth rates (CAGRs) through 2028
Highlights of the market potential and quantification of market based on therapy type, application, disease, and end-user
A look into current technologies underlying the market as well as the effects new technologies will have on the market
Coverage of clinical trials pipeline, partnership between pharmaceutical companies, and Contract Development & Manufacturing Organization (CDMO)
Insights into investments from multiple stakeholders, and discussion on increasing focus on personalized medicine for rare and chronic conditions
Information on recent mergers, acquisitions, collaborations, agreements, product launches, and expansions in the market and a relevant patent analysis
Company profiles of major players within the industry, including Catalent, Charles River Laboratories, Lonza, Merck KGaA, and Thermo Fisher Scientific
Chapter 1 Introduction
Study Goals and Objectives
Reasons for Doing This Study
Scope of Report
Information Sources
Methodology
Geographic Breakdown
Chapter 2 Summary and Highlights
Market Overview
Chapter 3 Market Overview and Technology Background
Overview
Gene Addition or Augmentation
Gene Correction
Gene Silencing
Manufacturing
Supply Chain
Regulatory Landscape
U.S. (FDA)
Europe
Outsourcing of Manufacturing
Chapter 4 Market Dynamics
Factors Affecting the Market
Market Drivers
Increasing Investment and Funding for CGT Development
Capacity Expansions for Clinical and Commercial Manufacturing
Rising Prevalence of Chronic Diseases and Focus on Rare Diseases
Increasing Strategic Collaborations and Acquisitions
Market Restraints
Complex Manufacturing and Supply Chain
Lack of Skilled Workforce
Regulatory Hurdles
Market Opportunities
Chapter 5 Emerging Technologies
Introduction
Emerging Technologies
Automation
Digitalization
Single-Use Technologies
Emerging Manufacturing Models
Chapter 6 Market Breakdown by Type
Overview
Cell Therapy
Gene Therapy
Cell Therapy Types
Autologous Cell Therapy
Allogeneic Cell Therapy
Cell and Gene Therapy Types Based on Vector Type
Viral Vectors
Nonviral Vectors
Chapter 7 Market Breakdown by Application
Overview
Clinical Manufacturing
Commercial Scale Manufacturing
Chapter 8 Market Breakdown by Disease
Overview
Cancer
Rare Diseases
Other Diseases
Chapter 9 Market Breakdown by End User
Overview
Pharmaceutical and Biotechnology Companies
Academic and Research Institutes
Others
Chapter 10 Market Breakdown by Region
Overview
North America
U.S.
Canada
Europe
U.K.
Germany
France
Rest of Europe
Asia-Pacific
China
Japan
Australia
Rest of Asia-Pacific
Rest of the World
Chapter 11 Sustainability: An ESG Perspective
Overview
ESG Practices in the CGT Manufacturing Industry
Case Studies: Examples of Successful ESG Implementation
Conclusion
Chapter 12 M&A, Funding Outlook and Competitive Landscape