by Kamile Gruduls | Jan 6, 2022 | EAEU, Regulatory Affairs, Webinar
Webinar: Smooth Switch to the EAEU Marketing Authorization for Medicinal Products The webinar will highlight the practical tips and guide you through the crucial steps of marketing authorization upgrade to the Eurasian Economic Union (EAEU) one, ultimately leading you...
by Nick | Oct 4, 2021 | Regulatory Affairs
Cultural and language problems are a frequent stumbling block for multinational corporations seeking to register drugs in Russia. Additionally, the Marketing Authorization process in Russia is highly complex, and the paperwork frequently changes as the regulatory...
by Nick | Aug 12, 2021 | EAEU, Regulatory Affairs
If you are interested in marketing your medicinal product in the fast-growing pharmaceutical market of the Eurasian Economic Union (EAEU) and if you want to how to apply for market authorization in the EAEU, this blog post is for you. The first part of this article...
by Kamile Gruduls | Jul 9, 2021 | Medical Devices, Regulatory Affairs
Since the establishment of the Eurasian Economic Union in 2015, a significant change is quickly coming into life: a new regional registration system for medical devices is coming into effect from the start of 2022. As most registrations are completed through national...
by Kamile Gruduls | Jun 17, 2021 | Medical Devices, Regulatory Affairs
EAEU legislation for Medical Device registration has been continuously updating for the last six years since the Eurasian Economic Union, otherwise known as EAEU, was entered into force in 2015. Five countries have signed the “Treaty on the Eurasian Economic...
