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Negócios · 29/07/20201 min de leitura
Postmarketing Safety Reports for Approved New Animal Drugs; Electronic Submission Requirements
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Resumo
The Food and Drug Administration (FDA, Agency, or we) is issuing a final rule to require electronic submission of certain postmarketing safety reports for approved new animal drugs. The final rule also provides a procedure for requesting a temporary waiver of the electronic submission requirement.
Idioma original da fonte: Federal Register — Food and Drug AdministrationAbrir o comunicado original →