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Imprese · 03/02/20161 min di lettura
Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application
Traduzione automatica locale · Lingua originale della fonte
Riepilogo
The Food and Drug Administration (FDA) is announcing that a collection of information entitled "Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application" has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
Lingua originale della fonte: Federal Register — Food and Drug AdministrationApri il comunicato originale →