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Zdrowie i gospodarka · 11/07/2017

FDA Requests Comments on Standardized Pharmaceutical Quality Data Elements and Terminologies

The US Food and Drug Administration (FDA) is seeking public comment on a draft standard for pharmaceutical quality data elements and terminologies, which could improve the efficiency and quality of the drug review process by transforming PQ/CMC submission data into a digital format.

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