you know our bureaucracy, everything but efficient ... Im guessing it will take a little bit longer because if you look at the gov approved tests, its largely antigen (very well known and not very new tech) , slightly less PCR, and only 1 entire kit - I think its Korean. Dotz RT-LAMP kit is the pinnacle of very new h-tech diagnostics technology, that the fda and their likes are less familiar with, so it makes sense investigation time takes longer, cause they have to familiarize themselves relatively from scratch...
but I think theres something important to notice here. you see these new drugs like Merck Regenron and the Pfizer one? these are ONLY USEFUL 72H-->5D since infection. Many people dont know they r sick in this timeframe, and also antigen tests are far less useful in the first 1-3 days - this is where errors occur. So for these medications to work, we need better systems of early detection, so much more PCR tests, and RT - LAMP that is to be honest, equally accurate and way more efficient in operationalization.https://pubmed.ncbi.nlm.nih.gov/32896179/
shit, sorry for the long preach mate. I get your point and largely agree, as someone in the field of biochemistry I think thats the sort of causal link behind..
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