Industry leading expertise in genetic design and optimization of cell and gene therapies.

Established clinical processes for donor cell enrichment, genetic modification, large scale cell expansion, and fill/freeze applicable to allogeneic and autologous cell therapies.

Robust operations for viral vectors to support cell therapies and extensive technical knowledge for in vivo gene delivery.

Streamlined processes, analytics and facilities for mammalian cell banking ideal for Research (RUO) and clinical (GMP) applications.

Ready with technical solutions for every stage of transfer.

Genuine partnership built on open interaction, rapid communication, and close alignment between our subject matter experts and our clients.