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Negócios · 29/03/20021 min de leitura
Agency Information Collection Activities; Announcement of OMB Approval; Medical Devices; Third-Party Premarket Submission Review and Quality System Inspections Under United States/European Community Mutual Recognition Agreement
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Resumo
The Food and Drug Administration (FDA) is announcing that a collection of information entitled "Medical Devices; Third-Party Premarket Submission Review and Quality System Inspections Under United States/European Community Mutual Recognition Agreement" has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
Idioma original da fonte: Federal Register — Food and Drug AdministrationAbrir o comunicado original →