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.
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.
