Processing joint Food and Drug Administration and European Medicines Agency voluntary genomic data submissions within the framework of the confidentiality arrangement
Current version |
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Published | 19/05/2006 |
Effective from | 19/05/2006 |
Keywords | Joint FDA-EMA voluntary genomic data submission (VGDS) |
Description | This document explains how the U.S. Food and Drug Administration and the European Medicines Agency will process requests for joint FDA-EMA voluntary genomic data submission (VGDS) briefing meetings. |