federal_register: E9-14907

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts regulation_id_numbers
E9-14907 The Essentials of Medical Device Regulations: A Primer for Manufacturers and Importers; Public Seminar Notice 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. 2009-06-24 2009 6 https://www.federalregister.gov/documents/2009/06/24/E9-14907/the-essentials-of-medical-device-regulations-a-primer-for-manufacturers-and-importers-public-seminar https://www.govinfo.gov/content/pkg/FR-2009-06-24/pdf/E9-14907.pdf Health and Human Services Department; Food and Drug Administration 221,199 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...  

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