Global Integrated Solution for cell therapy clinical development and commercialization

Download the eBook to walk through key considerations for developing a successful logistics strategy for the management of cell-based material.


Scalable Workflows

from manufacturer to patient administration

Cryogenic Distribution Expertise

in global advanced therapy clinical and commercial development

Global Innovative Solutions

for autologous and allogeneic cell therapies

The Connection between Strategy and Viability

The success of a advanced therapy clinical trial rests on the ability to deliver a viable, potent product. This positive end-result is directly attributable to the strategy in place and the supporting processes. A reliable advanced therapy logistics strategy is imperative to ensuring your biopharmaceutical products, therapeutic materials and patient biological samples remain viable from the point of manufacture to the final clinical site delivery.

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Global Clinical Trial Support

As the leading service provider to the cell and gene therapy community, Fisher Clinical Services is uniquely positioned with the experience, resources, and global expertise to support our customers on their path towards commercialization. Our global infrastructure enables customers to seamlessly conduct clinical trials across multiple geographies while providing patients around the world with access to life changing therapies. Our cryogenic storage and logistics, combined with proven components and validated procedures, allow us to configure and replicate each site to meet the specific requirements of individual clinical trials with minimal variation, regardless of volume or geographic location. This is supported by a global comprehensive and integrated Quality System based on regulatory requirements, industry best practices and trained personnel.

Navigating Unforeseen Challenges

Fisher Clinical Services can help you navigate many of the unforeseen challenges associated with advanced therapy clinical trials and the manufacture of biopharmaceutical products, which may directly impact product integrity, cost and scalability. We work collaboratively with our customers in every stage of development; from early phase trials through phase III, licensure, and global commercial distribution to develop state-of-the-art solutions. Our kit production services standardize the cell collection process; helping to maintain integrity and ensure quality pre-manufacture. We also provide expert assistance in storing biological and therapeutic materials and packing and transporting them to clinical and biopharmaceutical manufacture sites at cryogenic temperatures.

Configurable Workflows, Validated Processes

Our highly configurable advanced therapy workflows have the flexibility to address the unique requirements of your specific product, whether autologous or allogeneic. These workflows can be validated and standardized by our team of experts to ensure there is consistency in each and every cell collection or drug distribution that takes place. Through our tailored workflows and validation processes, we develop customized solutions to meet your needs and deliver your advanced therapy product safely and efficiently.

With experience maintaining the integrity of millions of samples in our global network of biorepositories, we are the experts in transporting, storing, and handling specialized biological samples and material. To learn more about how our services can support your projects select the icons below.

Supporting Services