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Zdrowie i gospodarka · 02/10/2015

FDA Releases Revised Draft Guidance on Common Technical Document-Efficacy

The US Food and Drug Administration (FDA) has made available a revised draft guidance on preparing efficacy components of pharmaceutical applications in the common technical document (CTD) format, as part of the International Conference on Harmonisation (ICH) efforts to standardize regulatory submissions.

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