1. Providing regulatory submissions in electronic and non-electronic format: promotional labeling and advertising materials for human prescription drugs Publication: Silver Spring, MD : Center for Drug Evaluation and Research, April 2022 Subject(s): Advertising -- legislation & jurisprudenceAdvertising -- standardsDrug ApprovalDrug Labeling -- legislation & jurisprudenceDrug Labeling -- standardsUnited StatesUnited States. Department of Health and Human ServicesUnited States. Food and Drug Administration
