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On March 10 th , the FDA issued guidance clarifying that 503A and 503B drug compounders must soon cease compounding semaglutide injection products[i] or risk enforcement action.[ii] This has a significant impact on compounding pharmacies as, under the Federal Food, Drug, and Cosmetic Act (the FD&C ), drug compounders are permitted to compound their own copies of a patented drug if the FDA determines it is in shortage

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(See the blog.) The NIHs RECOVER Initiative for long COVID demonstrated great initiative by using patient and physician reports to initiate a GLP-1 agonist

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