Cell and Gene Therapy CDMO Solutions

Achieve your critical drug development goals faster with global contract development and manufacturing (CDMO) facilities serving clients with research-grade and GMP plasmid DNA, viral vector, and cell therapy manufacturing.  Our integrated approach combines CMC, quality-by-design principles, and agile manufacturing processes to maximize knowledge transfer, reduce bottlenecks, and accelerate drug development.

scientists in PPE at our Memphis cell therapy CDMO center of excellence working in a cleanroom
Explore our Cell and Gene Therapy Manufacturing Services and Products
Plasmid DNA Manufacturing Services

Fit-for-purpose, platform-based plasmid production from research to High Quality and GMP grade, supporting all stages of clinical development through to commercial supply.

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Viral Vector Manufacturing Services

Development and scaled GMP manufacturing solutions for AAV, lentiviral vector, adenovirus, and retrovirus-based gene and gene-modified cell therapies.

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Cell Therapies CDMO Services

Analytical and process development and CGMP cell therapy manufacturing, services of autologous & allogenic T-cells, NKs, dendritic cells, MSCs, HSCs, and more,

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Off-the-Shelf Plasmid Products

Premium portfolio of off-the-shelf plasmid products to enhance and streamline gene therapy research and discovery programs.

Viral Vector Packaging Services

Customizable AAV packaging at multiple scales for every phase of research and custom lentiviral packaging for HQ and GMP grades.

CAR-T Manufacturing

Accelerate your CAR-T manufacturing program with a therapeutic development process built on quality, with custom assays, regulatory compliance, and robust manufacturing processes.

Quality and Regulatory Services

Our CDMO Center of Excellence in Memphis cleared back-to-back inspections by the European Medicines Agency and the Food and Drug Administration Center for Biologics Evaluation and Research.

Manufacturing Platforms

Proven production platforms to support streamlined plasmid DNA, viral vector, and CAR-T therapy manufacture with industry-leading timelines.

Oncology Manufacturing

Choose an oncology CDMO that removes complexity so you can advance therapies with confidence.

Cell and Gene Therapy CDMO Facilities

Accelerate the development of your product and ensure it meets the highest regulatory standards while maintaining efficient production timelines through our integrated global network of contract development and manufacturing organization (CDMO) facilities.

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Memphis

Cell Therapy Manufacturing: Memphis CDMO Site

Our cell therapy Center of Excellence in Memphis, TN, provides clinical and commercial manufacturing of cell and gene-modified cell therapies and recently passed back-to back inspections by the FDA and EMA for commercial drug manufacturing.
100,000 sq ft + 50,000 sq ft warehouse
265 employees
25 ISO 7 / Grade B suites
Good Manufacturing Practice (GMP)
Food and Drug Administration (FDA), USA
European Medicines Agency (EMA)
Health Canada
02
Keele

Plasmid DNA Manufacturing: Keele CDMO Site

Our plasmid Center of Excellence in Keele, UK, provides manufacturing of both research-grade and GMP plasmid. Quantities range from small quantities to support preclinical activities through bulk quantities for commercial cell therapy manufacturing.
15,000 sq ft + 3,229 warehouse
110 employees
10+ ISO 7 Grade C GMP production suites
Medicines and Healthcare products Regulatory Agency (MHRA) approved for Investigational Medicinal Products (IMP) production
Good Manufacturing Practice (GMP)
03
Rockville

Viral Vector Manufacturing: Rockville CDMO Site

Our viral vector Center of Excellence in Rockville, MD, provides manufacturing of research grade and GMP adeno-associated virus (AAV), lentiviral vector (LVV), adenovirus, and retrovirus for gene therapy and gene-modified cell therapies. Quantities range from small quantities to support preclinical activities through bulk quantities for commercial cell therapy manufacturing.
50,000 sq ft
130+ employees
8 production suites
Good Manufacturing Practice (GMP)
Food and Drug Administration (FDA), USA
European Medicines Agency (EMA)
Tell us about your program

Tell us about your program. Whether you need human immune and stem cell products or CDMO services that include process development, clinical manufacturing, or preparing for commercial scale, we are here to support you. Send us a message describing what you need, and we’ll connect you with the right team.

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