Saturday, March 13, 2021 2:08:41 PM
With over 60 years of SOC statistics, why select 400 patients to follow with paid healthcare (huge cost) just to say, we have a control group.
Some will say, it gives a truer test against current methods, but I find it hard to believe it's up to the sponsor to be burdened with this cost.
What's the FDA for, but to know current healthcare methods and outcomes, so they can decide if new methods are better. Don't they keep track of this?
If not, why? So they can slough off their job to bio companies trying to come up with life saving drugs.
Obviously, like Trump, I think the FDA is a old, slow dinosaur that only cares about itself and it's next job. They need to be taken apart, the millions of pages of useless processes examined by independent healthcare professionals, and what is that new term?
Reimagined.
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