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This means that the manufacturer should submit their data to the FDA to prove that the drug (or biological product) is safe and effective by conducting lab, animal, and human clinical testing for the drugs intended use

Maintenance phase Starting on day 15, the reserpine dose was reduced to 0.1 mg/kg and administered daily via i.p

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The pushback had a familiar flavour: You havent proved it doesnt work, and lack of human data doesnt mean lack of benefit. And "It's got a plausible mechanism." Heres my issue If you are going to claim efficacy (healing, belly fat loss, GH boosting, hypertrophy), you should be able to back that up with human trials for that claim, at that dose, with a defined product

So, what do you think: whats the biggest inefficiency youve seen in healthcare, and how did it impact patients or providers