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Zdrowie i gospodarka · 27/06/2019

FDA Releases Draft Guidance on Optimizing Safety Data Collection for Late-Stage Drug Studies

The FDA has made available a draft guidance from the International Council for Harmonisation (ICH) that recommends a selective approach to safety data collection in late-stage drug studies, aiming to advance clinical research and reduce patient burden.

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