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Negocios · 24/6/20091 min de lectura
The Essentials of Medical Device Regulations: A Primer for Manufacturers and Importers; Public Seminar
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Resumen
The Food and Drug Administration's (FDA's) Center for Devices and Radiological Health and Office of Regulatory Affairs, in cooperation with AdvaMed's Medical Technology Learning Institute, is announcing a series of three public seminars on FDA medical device regulations. These 2-day public seminars, which are designed to address the training needs of startup and small device manufacturers and their suppliers, will include both industry and FDA perspectives and a question and answer period.
Idioma original de la fuente: Federal Register — Food and Drug AdministrationAbrir el comunicado original →