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Psychol Med 2017;47:866-76

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Well, you lose early access You may lose cheaper options You lose access to compounds with marginal benefit that would not survive a formal development process Peter thinks what you gain is much more important Evidence, dose clarity, safety characterizations, manufacturing control, and post-market surveillance And that’s why he would have a hard time recommending non-approved peptides Not because FDA approval is infallible and final But because bypassing that system usually means giving up the information and oversight that you would need to make a defensible risk-benefit decision for yourself Why prescriptions from doctors, compounding pharmacies, and third-party testing do not validate unapproved peptides [A: 38:30, V: 36:48] Based on what you just said, if someone gets an unimproved peptide from either a doctor, a compounding pharmacy, or a vendor that has third-party testing, does that solve any of these problems