Zdrowie i gospodarka · 29/02/2012

FDA Announces Pilot Program for Electronic Submission of Nonclinical Study Data

The FDA is launching a pilot program to test the electronic submission of nonclinical study data using the Standard for Exchange of Nonclinical Data (SEND), a new electronic data standard format, to support review activity and evaluate its potential to streamline the submission process for investigational new drug applications (INDs).

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

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