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Zdrowie i gospodarka · 12/10/2017

FDA to Hold Public Meeting on Electronic Submissions and Data Standards Under Prescription Drug User Fee Act of 2017

The Food and Drug Administration (FDA) is hosting a public meeting to gather input from various stakeholders on electronic submissions and data standards, with the goal of improving the predictability and consistency of the electronic submissions process for human drug reviews.

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