Brazil Cell And Gene Therapy Cdmo Market Size & Outlook
The cell and gene therapy cdmo market in Brazil is expected to reach a projected revenue of US$ 370.2 million by 2033. A compound annual growth rate of 21.2% is expected of Brazil cell and gene therapy cdmo market from 2025 to 2033.
Brazil cell and gene therapy cdmo market highlights
The Brazil cell and gene therapy cdmo market generated a revenue of USD 67.4 million in 2024 and is expected to reach USD 370.2 million by 2033.
The Brazil market is expected to grow at a CAGR of 21.2% from 2025 to 2033.
In terms of segment, pre-clinical was the largest revenue generating phase in 2024.
Pre-clinical is the most lucrative phase segment registering the fastest growth during the forecast period.
Cell and gene therapy cdmo market data book summary
Market revenue in 2024
USD 67.4 million
Market revenue in 2033
USD 370.2 million
Growth rate
21.2% (CAGR from 2025 to 2033)
Largest segment
Pre-clinical
Fastest growing segment
Pre-clinical
Historical data
2021 - 2023
Base year
2024
Forecast period
2025 - 2033
Quantitative units
Revenue in USD million
Market segmentation
Pre-clinical, Clinical
Key market players worldwide
Lonza Group Ltd, Catalent Inc, Cytiva, Samsung Electronics Co Ltd, Thermo Fisher Scientific Inc, Novartis AG ADR, Wuxi AppTec Co Ltd, AGC Inc, OmniAb Inc, Rentschler Biopharma SE, Charles River Laboratories International Inc
Other key industry trends
In terms of revenue, Brazil accounted for 1.6% of the global cell and gene therapy cdmo market in 2024.
Country-wise, U.S. is expected to lead the global market in terms of revenue in 2033.
In Latin America, Brazil cell and gene therapy cdmo market is projected to lead the regional market in terms of revenue in 2033.
Brazil is the fastest growing regional market in Latin America and is projected to reach USD 370.2 million by 2033.
The robust growth & development in biologics and the rising biopharmaceutical market are expected to boost cell & gene therapy CDMO in the country. Moreover, the demand for cell and gene therapy CDMO in the country is growing as consumers increasingly seek effective biopharmaceutical formulations due to the growing burden of diseases.
The rising competition for drug development & approval is anticipated to increase the requirement for cell and gene therapy CDMO. Furthermore, government initiatives to reduce country’s pharmaceutical trade deficit and enhancement of domestic drug manufacturing are expected to boost the market.
For instance, in October 2023, Dipharma Francis S.R.L., a CDMO and major producer of APIs worldwide, announced that its manufacturing facility in Caronno Pertusella, close to Milan, Italy, has been granted the GMPcertification - Certificado de Boas Práticas de Fabricação (CBPF) - by Brazil's regulatory body Agência Nacional de Vigilância Sanitária (ANVISA). GMP certification from ANVISA enables Dipharma Francis S.R.L. to access the Brazilian pharmaceutical market, one of the largest in Latin America. This expands the company's market reach and potential client base
The databook is designed to serve as a comprehensive guide to navigating this sector. The databook focuses on market statistics denoted in the form of revenue and y-o-y growth and CAGR across the globe and regions. A detailed competitive and opportunity analyses related to Cell And Gene Therapy CDMO Market Outlook will help companies and investors design strategic landscapes.
Pre-Clinical was the largest segment with a revenue share of 78.64% in 2024.
Horizon Databook has segmented the Brazil cell and gene therapy cdmo market based on pre-clinical, clinical covering the revenue growth of each sub-segment from 2021 to 2033.
The robust growth & development in biologics and the rising biopharmaceutical market are expected to boost cell & gene therapy CDMO in the country. Moreover, the demand for cell and gene therapy CDMO in the country is growing as consumers increasingly seek effective biopharmaceutical formulations due to the growing burden of diseases.
The rising competition for drug development & approval is anticipated to increase the requirement for cell and gene therapy CDMO. Furthermore, government initiatives to reduce country’s pharmaceutical trade deficit and enhancement of domestic drug manufacturing are expected to boost the market.
For instance, in October 2023, Dipharma Francis S.R.L., a CDMO and major producer of APIs worldwide, announced that its manufacturing facility in Caronno Pertusella, close to Milan, Italy, has been granted the GMPcertification - Certificado de Boas Práticas de Fabricação (CBPF) - by Brazil's regulatory body Agência Nacional de Vigilância Sanitária (ANVISA). GMP certification from ANVISA enables Dipharma Francis S.R.L. to access the Brazilian pharmaceutical market, one of the largest in Latin America. This expands the company's market reach and potential client base
Brazil Cell And Gene Therapy Cdmo Market Phase Outlook (Revenue, USD Million , 2021-2033)
Pre-clinical
Clinical
Brazil Cell And Gene Therapy Cdmo Market Indication Outlook (Revenue, USD Million , 2021-2033)
Rare Diseases
Others
Oncology
Infectious Diseases
Neurological disorders
Brazil Cell And Gene Therapy Cdmo Market Product Type Outlook (Revenue, USD Million , 2021-2033)
Gene Therapy
Gene-Modified Cell Therapy
Cell Therapy
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Horizon Databook provides a detailed overview of country-level data and insights on the Brazil Cell And Gene Therapy CDMO Market Outlook, including forecasts for subscribers. This country databook contains high-level insights into Brazil Cell And Gene Therapy CDMO Market Outlook from 2021 to 2033, including revenue numbers, major trends, and company profiles.
Brazil Cell And Gene Therapy Cdmo Market, 2021-2033 (US$M)