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Russian and foreign legislation on regulation of post approval variations in the dossier for the medicinal products
Drug licensing is the most crucial factor for effective market regulation of pharmaceuticals. The rapid development of the pharmaceutical industry, emergence of new scientific data, and changes in composition of medicinal products drive the need for introduction of variations in original registratio...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Russo |
| Publicado: |
OOO “Vashe Tsifrovoe Izdatelstvo”
2018-02-01
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| Series: | Ведомости Научного центра экспертизы средств медицинского применения |
| Assuntos: | |
| Acceso en liña: | https://www.vedomostincesmp.ru/jour/article/view/58 |
| Tags: |
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