Imagine if there was an independent audit of FDA's decisions. I'm pretty sure they would not find batch to batch consistency. Maybe also quite a few potency problems. Not to mention the odd person without a clear ethical Mechanism of Action. I wonder how they would score on their ability to green light life saving and changing products to market for those that can not tolerate the side effects of traditional pharmaceuticals or for those where these pills have failed to stop the progression of disease?
Ann: Quarterly Activities/Appendix 4C Cash Flow Report, page-151
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