RE: Progress of LFD5 Sep 2020 18:50
DF......the following is a paragraph from 7th aug rns
LSTM is currently evaluating the performance of prototype lateral flow tests provided by Cytiva alongside Avacta's ELISA laboratory test using SARS-CoV-2 coronavirus samples, as a precursor to full clinical validation studies.
The following paragraph is from the 6th aug rns regarding BBI.
Avacta aims to begin clinical validation of the test as soon as possible by using the first pilot batches generated as part of the technology transfer process for these studies.
The following paragraph is from the 2nd sept rns regarding Abingdon.
Avacta aims to begin clinical validation of the test as soon as possible using the first pilot batches.
It looks to me that Cytiva produced some initial samples that have been sent to LSTM that have probably provided an early indication of S&S. These results will be used to assist Condors validation but this will not be completed until BBI produce the samples for them to evaluate and from the last rns it looks like this has not yet happened. Abingdon will only produce the validated product when it has been approved by Condor. I would think that as soon as the samples are produced the validation process will be fairly quick........after all it's a 10min test!