Cell and Gene Therapy Manufacturing QC Market is Expected to Drive Growth at a CAGR of 22.80% between 2020 and 2030

The global cell and gene therapy manufacturing QC market held a value of $574.8 million. The market is expected to grow at a CAGR of 22.80% during the forecast period 2020-2030 and attain a value of $5.92 billion by 2030. The growth in this market is primarily attributed to the rise in prevalence of cancer and chronic diseases and increase in investment from big pharma companies. In addition, the entry of several established players from the biomanufacturing market, such as Lonza AG and Merck KGaA, as well as diversification of product and service offerings among analytical testing juggernauts such as Charles River Laboratories International, Inc. and Eurofins Scientific SE, is aiding in tremendous market growth.

Market Segmentation

• Product – Services and Products (Kits and Assays, Instruments, Reagents, and Software)

• Process – Starting Material Preparation, Upstream Processing, and Downstream Processing

• Analytical Methods – Safety Testing, Purity Testing, Potency Testing, Identity Testing, and Stability Testing

• Technology – Polymerase Chain Reaction (PCR), Flow Cytometry, Limulus Amebocyte Lysate (LAL), Enzyme-Linked Immunosorbent Assay (ELISA), Chromatography, Mass Spectrometry, Western Blotting, Next-Generation Sequencing (NGS), and Electrophoresis, among others

Regional Segmentation

• North America – U.S., and Canada

• Europe – Germany, U.K., France, Italy, Spain, Netherlands, Russia, and Rest-of-Europe

• Asia-Pacific – China, Japan, India, Australia, South Korea, Singapore, and Rest-of-Asia-Pacific

• Latin America – Brazil, Mexico, and Rest-of-Latin America

• Rest-of-the-World

Growth Drivers

• Increasing Prevalence of Cancer and Chronic Diseases

• Rising Number of Clinical Trials

• Steady Investment and Consolidation in the Cell and Gene Therapy Market

• Favorable Regulatory Environment

Market Challenges

• Lack of Reliable Vector Production for Cell and Gene Therapy

• Lack of Therapy Specific Assays

Market Opportunities

• Drug Approvals and Strong Pipeline of Cell and Gene Therapies

• Multiple Investments in Expansion of cGMP Units

Key Companies Profiled

bioMérieux SA, Bio-Techne Corporation, Catalent, Inc., Charles River Laboratories International, Inc., Eurofins Scientific S.E., F. Hoffmann-La Roche Ltd., Intertek Group plc, Lonza Group AG, Merck KGaA, Sartorius AG, SGS S.A, Thermo Fisher Scientific Inc., WuXi AppTec, Sistemic Scotland Limited, and Vigene Biosciences, Inc.

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