Overview

Our Translational Cell Therapy Lab helps investigators establish clinically-relevant manufacturing processes and conduct the preclinical studies needed to bring cell therapy candidates to clinical trials.

Services offered include providing expert guidance on FDA testing requirements for cell products; assisting in preclinical research studies to assess the product’s safety and efficacy; and establishing processes to manufacture the product under conditions that meet the FDA’s rigorous Good Manufacturing Practices. 

By providing access to specialized facilities, staff and knowledge gained from projects that have already advanced through this translational stage, the TCTL accelerates the pace at which projects reach clinical readiness.  

Leadership

Services

Facilities

1,400-square-foot Good Laboratory Practice/Good Tissue Practice-compliant lab space

Resources

  • GMP-compatible induced pluripotent stem cell and embryonic stem cell banks
  • Inventory control (vendor qualification, warehousing and tracking)
  • Regulatory expertise
  • Quality assurance support
  • Assistance adapting a cell manufacturing protocol to Good Manufacturing Practices
  • Assistance with qualification of analytical assays
  • Training on manufacturing and regulatory topics specific to cell and gene therapy products