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National Law Review (Polsinelli PC) was explicit on April 22, 2026: removing a Category 2 bulk drug substance does not, on its own, authorize use of that substance in compounding or bring it within FDAs interim enforcement discretion policy for substances in Category 1. Even Category 1 substances are only under enforcement discretion, which is short of full authorization

Clinical research priorities include properly designed human clinical trials with adequate sample sizes, appropriate controls, and validated outcome measures

3 ingredients