Requirement for producer cell line for GMP viral vector packaging
NHS Blood and Transplant · United Kingdom
Key facts
- Contract value
- £111,000
- Awarded
- 06 Apr 2022
- Contract starts
- 06 Apr 2022
- Contract ends
- 05 Apr 2024
- Procedure
- Open procedure (above threshold)
- Buyer type
- Health
Awarded to
| Supplier | Value |
|---|---|
| Life Technologies Ltd | £111,000 |
Description
NHSBT's Clinical Biotechnology Centre for the purpose of specifying the user requirement for HEK293-derived production cell line for the GMP-production of viral vectors and other recombinant proteins. The CBC has an MHRA licence for the manufacture of investigational medicinal gene therapy and recombinant protein products for use in clinical trials. In order to manufacture GMP-grade viral vectors and recombinant proteins for clinical trials, a GMP-qualified producer cell line is required.
Categories (CPV)
- 33141000 Disposable non-chemical medical consumables and haematological consumables
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