GMP Manufacturing

Fill Finish

We offer flexible, GMP-compliant fill finish services for viral vectors, allogeneic cell therapies and other biotechnology products. Whether integrated or standalone, our approach ensures quality, containment, and clinical readiness.

Deliver Clinical-Grade Product with Confidence

Fill finish is a critical step in preparing cell and gene therapies for clinical trials. Errors or inconsistencies at this stage can impact sterility, dose accuracy, and patient safety. For many early stage clinical developers accessing GMP fill finish capacity is a barrier, particularly when looking for standalone services.

Our dedicated fill finish module allows us to support fill finish as a standalone offering or as part of a wider manufacturing programme. This flexibility helps de-risk your supply chain and keep clinical timelines on track.

Our Approach

Our GMP facility includes a dedicated fill finish module comprising a Grade C cleanroom and a closed Grade A isolator system. This setup supports clinical-stage filling of viral vectors and allogeneic cell therapies into pre-sterilised vials or bags, with capacity for up to 500 vials per shift (dependent on fill volume and configuration).

Our Filling equipment is designed to accommodate a range of fill/finish needs using ready sterilised filling components. Our isolator can accommodate the Aspetic Technologies M1 filler if required.  All activities are managed under GMP conditions with full quality oversight and documentation. We also offer process development and validation support where required.

Secure GMP Fill Finish Without the Wait

Our standalone and integrated fill finish services help keep your clinical timelines on track. Contact us today to discuss your fill finish requirements.