Monday, March 01, 2021 4:49:27 PM
I'm already rich.
"How many strains does it detect?"
I don't know and I don't care.
"What is the sensitivity and specitivity readouts? "
Once again I don't care.
"Wouldn't that be public information the EU would disclose? "
Once again I really don't care.
It is my understanding that getting a CE Mark is much easier that an FDA approval. Generally as long as it does no harm its good to go. For FDA you have to prove efficacy. That's why all the good stuff ends up in Europe first. I am confident that all my information is incorrect and all the experts on this board will know absolutely everything there is to know about getting a CE Mark. If you are giving the CE Mark the same requirements as FDA I might suggest you do a bit more research.
For the record it no longer matters about the money, it's a whole different thing.
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