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