Quote:
Originally Posted by blankall
My understanding was it was the opposite.
Phase I was where most of the safety issues were dealt with. Phase III is for ensuring effectiveness on a mass scale.
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I'm no expert, but this doesn't seem to make sense, does it? Don't they have to monkey with it and tweak things to get it to maximum effectiveness? If so, wouldn't you have to re-do the safety tests on the tweaked version to ensure your changes didn't result in adverse health risks?
I dunno, maybe someone who knows about this process can weigh in.