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503B Reporting: AERs
Human Drug Compounding Under Sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act
503B Adverse Event Reporting Guidance
503B Reporting: AERs
OMB: 0910-0800
OMB.report
HHS/FDA
OMB 0910-0800
ICR 202210-0910-015
IC 217571
503B Reporting: AERs
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