Cell and Gene Therapies
Tailored solutions for cell and gene therapy programs.
Expertise and services to amplify your clinical trial approaches, streamline complex processes and minimize risk.
Strategic support
Access multidisciplinary, multimodality experience to support your studies.
Centered on patients
Get a patient-centric approach to optimize the development of your product.
Expert problem-solving
Rely on our team to navigate complex logistics and implement practical solutions.
Reduce risk for your cell and gene studies
Fortrea delivers strategic insights to enable efficient, cost-effective development of your cell and gene therapies and reduce risk across critical milestones. Our expertise across multiple modalities, clinical conduct insights, operational solutions and customized training enable us to deliver the experience you need for your study.
Enable seamless delivery
Apply our know-how and infrastructure
-
Expertise with multiple modalities
- CAR T and AAV
- Other viral and nonviral delivery systems (e.g., adenovirus, LNP)
- Cell therapies (immune cell/stem cell, autologous/allogeneic, modified/non-modified)
- Gene editing (e.g., CRISPR, meganucleases)
- Advanced and complex therapeutics such as RNA-based therapies (e.g., ASOs, siRNAs), T-cell engagers and genetically modified organisms
-
Scientific and medical insights
-
Global operational solutions
-
Customized training
Cell and gene therapy experience that matters
In the last 5 years, we have supported:
Advance your cell therapy studies
Fortrea has supported and designed dozens of cell therapy programs, including all 6 FDA-approved CAR T-cell therapies.


Global gene therapy experience
No matter where you are or where you intend to go, you can rely on our global experience and expertise in advancing gene therapy trials.
Oncology in cell and gene therapy development
From targeted therapies and immunotherapies to advanced cell and gene therapies, we have helped develop biomarker-driven strategies to bring precision medicines to market.

Insights