Expert personnel in a fully licensed environment

With our world leading experts in the field of GMP, we are in position to support each study with dedicated teams of production and quality control, led by Heads of Advanced Therapy Production and Quality, and Qualified Persons specialising in ATMPs.

Medicines and Health Products Regulatory Agency (MHRA)

MIA (IMP) Licence Cell or gene therapies for use in clinical trials are manufactured under MIA (IMP) Licence (Manufacturers Authorisation for Investigational Medicinal Products).

Specials Licence (MS) We hold an MS licence for the manufacture and supply of unlicensed ATMPs for human use outside of clinical trial settings.


Human Tissue Authority (HTA)

We are authorised for these licensable activities:


  • Procurement
  • Donor testing
  • Processing of tissue and cells


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