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Plan for Success in Gene and Cell Therapy Manufacturing

Cell Therapy
Credit : Istock

In the last decade, gene and cell therapies have been transformed from a clinical concept into a therapeutic reality. Interest in these new treatment options remains strong, despite the challenges associated with their production.

When developing these therapeutics viral vectors are used to deliver genetic material into cells. Producing and characterizing these vectors can be costly, time-consuming, and subject to rigorous regulatory scrutiny. Overcoming these hurdles requires careful planning and preparation during the manufacturing process. 

This whitepaper highlights essential factors to consider for the successful manufacturing of gene and cell therapies.

Download this whitepaper to learn how to:

  • Choose a reliable plasmid DNA provider
  • Establish a target product profile
  • Effectively design optimal plasmids for your experiment

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