
The general assembly of the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) has adopted a new topic focused on the harmonization of bioequivalence for modified-release products.
This event took place at the ICH meeting in Vancouver, Canada, marking the introduction of a new ICH multidisciplinary guideline, which aims to further strengthen consensus and harmonization among ICH members regarding bioequivalence standards for more complex dosage forms.
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