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Negócios · 08/03/19991 min de leitura
Agency Information Collection Activities; Announcement of OMB Approval; Medical Devices: Third-Party Review Program Under the U.S./EC MRA
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Resumo
The Food and Drug Administration (FDA) is announcing that a collection of information entitled ``Medical Devices: Third-Party Review Program Under the U.S./EC MRA'' 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 →