Specialist technologies supporting ATMP research include peripheral blood mononuclear cell (PBMC) processing facilities, a purpose-built aseptic dispensing laboratory for ATIMP preparation, and access to advanced imaging and diagnostic services. These are complemented by the Clinical Research Centre, offering dedicated clinical and procedural space for complex study visits.

Clinical research is embedded into routine patient pathways across NHS Tayside. Major specialties incorporate review of research opportunities into weekly MDT discussions, ensuring equitable access for eligible patients and supporting strong recruitment performance.

NHS Tayside has over 20 years of experience delivering ATMP studies and continues to expand its portfolio of commercial and non-commercial advanced therapy trials. Our governance structures, specialist facilities, biosafety expertise, and agile research workforce provide a robust and adaptable framework for safe, compliant delivery of ATMP studies across a broad range of clinical areas. NHS Tayside is also Health and Safety Executive (HSE)- registered for gene therapy delivery.

ATMP activity is governed by our Advanced Therapy and Gene Modification Safety Committee (ATGMSC), which provides expert biosafety and capacity assessments for all proposed studies. The committee supports streamlined approvals and is underpinned by two trained Biosafety Officers and a dedicated ATIMP Research Nurse completing advanced biosafety training. This specialist oversight ensures robust risk assessment and safe delivery of gene- and cell-based therapies.