Regulatory requirements of the European Medicines Agency for evaluation of bioequivalence of modified-release medicinal products

There are no specific requirements and recommendations in the Russian Federation for evaluation of bioequivalence of modified-release medicinal products. Until recently, modified-release products were regulated in a similar manner as immediate-release products, which is unacceptable considering the...

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Bibliographic Details
Main Authors: D. P. Romodanovsky, N. N. Eremenko, D. V. Goryachev
Format: Article
Language:Russian
Published: OOO “Vashe Tsifrovoe Izdatelstvo” 2019-03-01
Series:Ведомости Научного центра экспертизы средств медицинского применения
Subjects:
Online Access:https://www.vedomostincesmp.ru/jour/article/view/218