RE: FDA Approval14 May 2022 14:20
Hi BucksLad
'Clearly Angle board assumes its now just a buereaucratic delay caused by initial lack of reagents and covid absences at the FDA labs and office.'
The lack of reagents has nothing to do with the FDA approval. It relates to the analysis of the samples in the ovarian trial. Regarding the FDA labs, I am not aware that the FDA are undertaking their own hands on trial of Parsortix and the company have never indicated that this is taking place, so I think you are perhaps mistaken on this. The impact of Covid has no doubt delayed things.