1. Providing regulatory submissions in alternate electronic format Publication: Silver Spring, MD : Center for Drug Evaluation and Research, July 2021 Subject(s): Biological ProductsDrug ApprovalDrug DevelopmentElectronic MailGovernment RegulationUnited StatesUnited States. Department of Health and Human ServicesUnited States. Food and Drug Administration
2. Providing submissions in electronic format: postmarketing safety reports Publication: Silver Spring, MD : Center for Drug Evaluation and Research, April 2022 Subject(s): Drug ApprovalElectronic MailProduct Surveillance, PostmarketingUnited StatesUnited States. Department of Health and Human ServicesUnited States. Food and Drug Administration
