Translational guidance
Guiding our collaborators through the translational journey from bench to bedside.
Off
Bridging the “translational gap” to turn promising research into medicines requires multidisciplinary capabilities. The team at the Gene Therapy Innovation and Manufacturing Centre (GTIMC) utilises multidisciplinary regulatory expertise to:
- advise on the final clinical configuration of the therapeutic vector before initiating manufacturing. This will ensure alignment with safety and regulatory aspects;
- help with the design of good laboratory practice (GLP) preclinical studies;
- develop data for regulatory submission.
If you are looking for guidance on progressing your laboratory based gene therapy research along the translational pathway, contact us: gtimc@sheffield.ac.uk