Who plays what role?23 Aug 2020 15:18
Can I just check my (basic) understanding of the current players and their roles?
-Avacta - make the affimers that are central to the test
-Cytiva - create and optimise the membrane, create a prototype, and produce manufacturing procedures for the test. Produce analytical validation of the test.
-BBI - lead manufacturer. Appointed to develop and validate a scaled up manufacturing process, ie to take the process Cytiva give them, stick a rocket under it to create volume, use the process to make it themselves, and (hopefully) transfer that scaled up process to other manufacturers (yet to be announced).
-CONDOR - assist with rapid clinical validation of pilot batch tests produced by BBI
-LSTM - also assisting in clinical validation through access to additional live samples
- Medusa19 - exclusive B2C distributor. Can also supply businesses
-Saturn Passport - not really sure they have anything to do with us directly
So, if this is all correct (it may not be!), then the clinical validation is being completed at the same time that BBI are finalising the manufacturing scale up process, such that we should be in a position to produce through BBI as soon as the validation is complete. We are hoping that govt procurement talks will be at a very advanced if not final stage by that same time, and that they will be buying the first batches. I’m assuming we would then name other manufacturing partners and transfer the scaled up BBI process to them, so that we can meet the anticipated very high global demand.
Would be grateful if anyone can tell me if this is right or wrong...
Thx