Streamline the path from discovery to cure

As you move your translational stem cell, tissue engineering, and immunotherapy research toward the clinic, your product selection, lab process, documentation, and quality assurance steps become more demanding. This collection of resources will help you gain a better understanding of cell therapy research, feel confident at every step, and maximize your time, effort, and outcomes.

Featured resources

CTS Mini-documentary series

In this 7-part series, hear from four experts with backgrounds in stem cell therapy and immunotherapy research, cell therapy manufacturing, and clinical development on their unique perspectives on the opportunities and challenges facing the cell therapy industry.


Webinar: New viral and non-viral platforms for T-cell engineering

In this webinar, we will highlight the different viral and non-viral delivery approaches used in T cell engineering for cell and gene therapy applications including LV-MAX Lentiviral Production System and novel gene editing tools for primary T cells.

Webinar: Comparison of the Teratoma assay and in vitro surrogate tests for assessment of pluripotency of human pluripotent stem cells

For optimal use of human induced pluripotent stem cells (hiPSCs) it is essential to identify lines that are fully reprogrammed and of high quality with proven pluripotency in terms of differentiation. This presentation will compare different solutions for the assessment of that pluripotency.

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Type Name
Brochure Advanced therapy brochure 
Brochure Cell therapy selection guide 
Brochure Cell therapy solutions brochure 
Brochure Cell therapy systems (CTS): Products to help you move your research toward the clinic 
Brochure Immunotherapy brochure 
Brochure Immuno-oncology brochure 
Brochure Lentiviral production capabilities brochure 
Brochure Mesenchymal stem cell resource guide
Brochure Pluripotent stem cell products and services guidebook 
FAQ Cell therapy systems (CTS) frequently asked questions 
FAQ CTS clinical/commerical use frequently asked questions
FAQ CTS immune cell SR for serum free culture and expansion of human T cells 
FAQ Ex vivo expansion of human T cells for adoptive immunotherapy using the novel xeno-free CTS immune cell serum replacement 
Handbook Pluripotent stem cell handbook
Literature Case study: Reducing cost within advanced therapy clinical trials 
Literature eBook: Cell therapy logistics beyond the basics 
Literature eBook: QP essentials: EU gateway to clinical and commercial distribution of cell therapeutics 
Literature eBook: Commercially successful cell therapies: Navigating the ultra cold chain distribution minefield 
Poster A Sendai viral reprogramming kit for completely xeno-free generation of iPSC 
Poster Large scale serum free suspension lentiviral production system for gene therapy application 
Publication A rapid cell expansion process for production of engineered autologous CAR-T cell therapies 
Webinar Thermo Fisher Scientific cell therapy capabilities 
Webinar Improved T cell function and in vivo engraftment of CAR-T cells 
Webinar Comparison of the Teratoma assay and in vitro surrogate tests for assessment of pluripotency of human pluripotent stem cells 
Webinar Comprehensive characterization of pluripotent stem cells 
Webinar Optimizing advanced therapy supply chain design to ensure commercial success >
Webinar Cell therapy: Achieving success on the road to commercialization 
Webinar Comparison of the Teratoma assay and in vitro surrogate tests for assessment of pluripotency of human pluripotent stem cells 
Webinar New viral and non-viral platforms for T-cell engineering 
Webinar Transitioning to the clinic from proof of concept research 
Video Translating cell therapy research into clinical success: A Gibco CTS mini-documentary series 
Video Eliminate serum to gain control of your T cell research – New xenofree serum replacement 

Cell therapy systems (CTS) products

The CTS product line is designed for use in cell therapy research applications and includes media, reagents, growth factors, enzymes, selection beads, and devices, which are manufactured in compliance with 21 CFR Part 820 Quality System Regulation and/or are certified to ISO 13485 and ISO 9001.