Unlock Your Partnership with a License Tailored to Your Development Goals

Discover how a MaxCyte license provides a strategic advantage in the evolving cell and gene therapy landscape. With cutting-edge technology, tailored financial flexibility, unmatched transparency, and dedicated partnership support, MaxCyte empowers innovators to accelerate discovery, scale-out, and commercialization with confidence.

Explore the difference a MaxCyte partnership makes in advancing transformative therapies.

Unlock the potential of your cell and gene therapy programs with a MaxCyte license—a proven pathway to development with unparalleled support. By aligning with your unique goals, your tailored MaxCyte's license empowers you to navigate every stage, from clinical development to commercialization, with confidence. Access best-in-class technology, scalable GMP-compliant processes, regulatory guidance, 24/7 manufacturing assistance, and lead-time guarantees.

Accelerate your pathway to development with upfront investment from MaxCyte at no additional cost, only after you reach the clinic does our win-win licensing model take effect. With MaxCyte, licensing is more than a contract —it's your strategic advantage designed to advance transformative therapies with transparency and trust.

Inside the License: Unlocking Your Competitive Edge

Best-in-class Technology and Optimized Protocols

Proven platform technology ensures high transfection efficiency, scalability, and reproducibility across phases.

Achieve consistent, scalable results while saving months of optimization and reducing development costs.

Process Optimization and Transfer Support

Dedicated expertise for onsite process optimization and seamless process transfer, ensuring consistency and efficiency across development stages.

Streamline scale-up and transfer processes, saving months of development time and reducing associated costs.

Comprehensive Engineering Services

Warranty-backed maintenance, troubleshooting, and repair to minimize downtime and ensure reliability.

Maximize system uptime and ensure smooth operations during critical development stages.

Regulatory and Compliance Support

FDA Master File and global technical files supporting first approved non-viral therapy and over 60 clinical trials.

Streamline regulatory submissions and minimize risks, accelerating clinical and commercial success.

Cumulative Expertise and Know-How

25 years of cell therapy experience to optimize processes and ensure regulatory readiness.

Accelerate milestones with expert guidance and proven solutions tailored to your needs.

Supply and Lead Time Guarantees

Reliable supply and guaranteed lead times for instruments and consumables to ensure uninterrupted progress for your programs.

Ensure seamless operations with no delays or disruptions, enabling you to meet critical milestones on time.

Unlock Exceptional Results with MaxCyte's Scientific Expertise and Support

Partner with MaxCyte scientists to confidently navigate your pathway to discovery, leveraging expert support and unlocking transformative results.

Andrew shares how his collaboration with a cell-therapy developer led to a 90% efficiency boost, enabling the developer to confidently proceed with clinical manufacturing.

Hear from Andrew

Hear how Megan identified a critical flaw in the technology transfer process from a customer to a CDMO. Her swift action ensured a timely resolution and improved standard operating procedures.

Hear from Megan

Hear from Joan as she shares how her dedication and scientific expertise helped a stealth mode cell therapy company overcome a critical challenge and successfully reach their next inflection point.

Hear from Joan

Listen to Peter go through how he helped a partner overcome challenges in scaling up their cell therapy process using our large-scale electroporation platform, so they could produce and cryopreserve one batch for multiple doses.

Hear from Peter

Ready to streamline your cell therapy pathway to development?

Contact our Business Development team today

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