Research design formation to determine quality indicators of potential api, 2. quality risks arising in the process of scaling the synthesis procedure

Within the framework of the current pharmaceutical legislation, harmonized as much as possible with the EU and the USA to ensure the import / export of high-quality medicines (within the framework of the ICH and the positions of the global pharmaceutical sector), the transfer of technology for obtai...

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Bibliographic Details
Main Authors: Nataliia Bevz, Volodymyr Mishchenko, Viktor Khomenko, Victoriya Georgiyants
Format: Article
Language:English
Published: PC Technology Center 2020-12-01
Series:ScienceRise: Pharmaceutical Science
Subjects:
Online Access:http://journals.uran.ua/sr_pharm/article/view/221940