Recommendations on the EAEU Marketing Authorisation Procedures to Optimise the Performance of Regulatory Affairs Specialists
Since 2021, the marketing authorisation (MA) of new medicinal products in the Russian Federation has been carried out according to the Rules of Marketing Authorisation and Assessment of Medicinal Products for Human Use that are implemented by Decision No. 78 of the Council of the Eurasian Economic C...
| Main Authors: | , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
NEICON ISP LLC
2023-07-01
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| Series: | Ведомости Научного центра экспертизы средств медицинского применения |
| Subjects: | |
| Online Access: | https://www.vedomostincesmp.ru/jour/article/view/544 |