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31.05.2023
REGULATIONS ON LICENSING THE MANUFACTURING OF MEDICINES HAS BEEN UPDATED
It is clarified that confirmation of compliance of a licence applicant and a licensee with the requirements of the rules of good manufacturing practice of the EAEU should be carried out within the framework of licensing the manufacturing of medicines, including when making changes to the register of licences. 
The requirement concerning an enhanced qualified digital signature when sending an application for a licence to the licensing authority has been eliminated.
 

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