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Zdrowie i gospodarka · 17/07/1996

FDA Publishes ICH Guideline for Clinical Study Reports

The FDA has released a new guideline to standardize the structure and content of clinical study reports, aiming to facilitate a single, globally accepted report for regulatory authorities, under the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use.

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