Regulatory Strategy in the EAEU and rest of CIS Countries

Webinar: Regulatory Strategy in the EAEU and Rest of CIS Countries

Regulatory strategy in EAEU and CIS regions differ from other regions as market access to these countries can be a real challenge due to various local regulations. However, it is only a matter of experience and adequate know-how.

This webinar focuses on choosing your regulatory strategy for Eurasian Economic Union and Commonwealth of Independent States, best practices and practical tips for market access and current regulatory status and GMP requirements.

 

You will learn about:

1. Commonwealth of Independent States

  • Differences and overlaps with EAEU

2. Regulatory strategy in the EAEU

  • Current status and main challenges
  • Practical tips

3. Regulatory strategy in the CIS region

  • What is the current status?
  • Best practices and key tips for main challenges
  • GMP requirements in EAEU and CIS

 

Entering EAEU or CIS markets?

Make use of our experts’ know-how to access new markets. Explore your options in a chat with one of our experts.

Who should attend?

  • Global and regional RA Managers
  • Regulatory Strategy Managers
  • RA Partnerships Operations Manager
  • QA Managers supporting RA
  • RA Healthcare Compliance Managers

Duration: 25 min.

Speaker: Regulatory Affairs Project Manager, Nargiz Asgarova, who will share her expertise on regulatory strategy in EAEU and CIS regions.

Nargiz Asgarova, BSc, MBA

Nargiz Asgarova, BSc, MBA

Regulatory Affairs Project Manager

Other content that might interest you:

Running A Clinical Trial In Georgia

Running A Clinical Trial In Georgia

Moving Clinical Trials away from Ukraine and Russia Russia, Ukraine, and other CIS countries have been significant contributors to clinical trials in many therapeutic areas for several years. With access to experienced investigators, good quality, and large patient...

read more

Big Enough To Cover  All Your Needs. Small Enough To Care.

Discover the tailored solutions that Biomapas provides to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Regulatory Affairs

Pharmacovigilance

Medical Information