Cell Therapy Research Services

It is possible to reduce the time and cost of developing a new cellular therapy by considering the requirements of GMP manufacturing at an early stage in the project. 

We consider planning for eventual GMP manufacture to be an integral part of any cell therapy research project, and are pleased to be able to offer the following services for early-stage projects:

  • SOP development support and approval
  • Production of Investigational Medicinal Product Dossier (IMPD)
  • Process validation, advice and guidance, practical application
  • Support in writing grant applications including GMP manufacturing
  • GMP Training
  • Facility & Process audits
  • Product/Process Specification Development
  • Tissue Culture Procedures
  • Tissue/Cell isolation
  • Cryopreservation
  • Environmental Monitoring (viable/non-viable)
  • Product QC testing
  • Critical material qualification and controlled storage