Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union

The Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union is dedicated to the developments in pharmaceutical regulatory affairs in Russia, the Eurasian Union and the CIS.

Key Topics

• Essential information on the latest regulations and registration procedures in the Eurasian Customs Union
• The competitive landscape of the growing markets in the CIS region
• CIS Regional Submission Plan and its place within the global regulatory strategy
• National requirements and guidance for drug approval in the core CIS markets of Russia, Kazakhstan, Belarus, Ukraine and Azerbaijan
• Implications of the new regulations which will affect how you do business in the Eurasian Economic Union (EAEU)
• Full background to the CIS pharmaceutical market
• National regulations in Russia, Belarus, Kazakhstan, Ukraine and other CIS countries
• Document requirements and timelines of national procedures and EAEU registration procedures

Who should Attend

Attendees involved or interested in pharmaceutical regulatory affairs in this region.