Cette traduction est en cours de préparation. En attendant, nous affichons temporairement la version originale en anglais.
Entreprise · 24/06/20091 min de lecture
The Essentials of Medical Device Regulations: A Primer for Manufacturers and Importers; Public Seminar
Traduction automatique locale · Langue originale de la source
Résumé
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.
Langue originale de la source: Federal Register — Food and Drug AdministrationOuvrir le communiqué original →