OVERVIEW

Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union Training Course is organized by Management Forum (Mf) Ltd and will be held from Feb 04 - 05, 2021.

Who should attend?
This seminar will be of particular interest to all those who need to learn about successful marketing authorisation applications and regulatory compliance in this region. The seminar will be useful either as an introductory or refresher course.

Accreditation:
This course qualifies for 12 hours for your CPD records.

Course Overview:
The pharmaceutical markets in Russia, the Eurasian Union and the CIS are of growing commercial importance and companies looking to take advantage of the opportunities available need to be fully up to date with the evolving regulatory landscape, including the potential for market access offered by the latest legislation.

This interactive course will guide you through national procedures as well as exploring the implications of and updates on the Eurasian Union regulation.

The focus of the programme is to offer practical advice in developing your regulatory strategy for product approval in these countries and you will get the full benefit of our trainer’s experience and expertise in the region.

Benefits of attending:
• Understand the competitive landscape of the growing markets in the CIS region
• Discover the essential information on the latest regulations and registration procedures in the Eurasian Customs Union
• Discuss national requirements and guidance for drug approval in the core CIS markets of Russia, Kazakhstan, Belarus, Ukraine and Azerbaijan
• Develop your CIS regional submission plan and place it within your global regulatory strategy
• Gain practical advice from an industry expert working in the the CIS region

Why you should attend:
Attending this programme will:
• Give you the full background to the CIS pharmaceutical market
• Ensure that you understand all the implications of the latest regulations which will affect how you do business in the Eurasian Economic Union (EAEU)
• Help clarify the document requirements and timelines of national procedures and EAEU registration procedures
• Update you on the national regulations in Russia, Belarus, Kazakhstan, Ukraine and other CIS countries