Continuous mRNA manufacturing to boost therapy and vaccine output
New mRNA-based therapies and vaccines could be developed more quickly and cheaply thanks to new manufacturing technologies developed at the University of Sheffield
New mRNA-based therapies and vaccines could be developed more quickly and cheaply thanks to new manufacturing technologies developed at the University of Sheffield
Hear from leading scientists how they are bringing the promise of customized medicine to life, and discover the key players in an industry that is shaping the future of cell and gene therapy
Explore how a nascent method for the precise production of CAR-T cells could pave the way for the next generation of cancer assassins
Discover how the Wellcome Sanger Institute is helping to develop a physical atlas of all human organs
Explore how the latest advancements and recent regulatory approvals are making truly personalized medicine a reality
As we celebrate the first regulatory approval of a gene-editing based therapeutic, Casgevy™, for the treatment of sickle cell disease and transfusion-dependent β-thalassemia, we consider the gene-editing challenges that must be overcome before CRISPR gene-editing technology becomes a common treatment modality
Agilent Technologies, Thermo Fisher Scientific, and Tecan among those recognized
Experts at the University of Nottingham have discovered how to create different colors of blue cheese
Discover which products have earned a coveted Seal of Quality award
New study findings from the University of Manchester are important for the development of new wound therapies
Visit our new Cell and Gene Therapy Accelerating Science feature to explore the remarkable achievements in the field and investigate the possibilities ahead
Discover the latest webinars, methods and products in gene editing technology
Casgevy™ and Lyfgenia™ approvals pave the way for personalized gene editing therapies in treating sickle cell disease
Discover the impact of mass photometry in AAV process development in this exclusive interview with a viral vector expert
For the chance to win a $500 Amazon Gift Card (or equivalent currency) cast your vote for the new product that has made the most difference to research
Learn how researchers are using innovative gene editing techniques to uncover new drug targets
Explore the latest developments in cancer research with fellow scientists, manufacturers, and regulatory experts
This special feature highlights interviews and resources about the latest advances in cell and gene therapy and the technologies behind them
Experts discuss how to navigate the frontier of cell and gene therapy for the treatment of cancer
Experienced commercial leader to lead strategic expansion of Cresset's molecular modeling expertise and solutions
The first RNA-guided DNA-cutting enzyme found in eukaryotes, Fanzor could one day be harnessed to edit DNA more precisely than CRISPR/Cas systems