The regulatory authorities are flawed because they are accepting overseas RATS within 3 - 5 days based on manufactures word, in contrast to the 3 month well get back to you with need more information.
They started "working with us" after the media and finally gave us a straight answer that we need two trials with X samples in Y condition.
Also why does Anteotech have to do two trials? Why is one trial is not sufficient? Is that because there is more likely to be different variants? Okay fine, what about the self RATS that were approved without trails confirming they can detect variants?
Something very off with the TGA.
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