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Zdrowie i gospodarka · 24/09/1999

FDA Publishes Draft Guidance on Choosing Control Groups in Clinical Trials for Human Use

The FDA is releasing a draft guidance document, E10, to help sponsors and investigators select control groups for clinical trials intended to show drug efficacy, in collaboration with the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH).

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