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Zdrowie i gospodarka · 07/05/2019

FDA Announces Final Guidance for Medical Device Submissions Feedback and Meetings

The Food and Drug Administration (FDA) has released a final guidance document outlining the procedures for requesting feedback and meetings with the FDA regarding various medical device submissions, including IDE, PMAs, HDEs, De Novo requests, 510(k) submissions, and IND applications.

Source: Federal Register — Food and Drug AdministrationOpen original release →