This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

6th - 8th April 2022
★ 100% virtual conference ★Presented in Central European Time (CET)

APAC, LATAM, MENA, CIS: Unlock Accelerated Regulatory Pathways, Break Into New Markets and Maintain Global Compliance

Keep Up With The Fast-Evolving Market Access Requirements With Direct Guidance From Government Bodies and Pharmaceutical Regulatory Leaders

Including Harmonisation Efforts, China's Drug Administration Law, The Impact of COVID-19 And Much More

Obtain updates from government bodies and industry to get one step closer to breaking into:


  • Delve into China’s Drug Administration Law with Menarini Ricerche   
  • Hear experiences with Market Authorisation in China with Chiesi Group   
  • Get updates into ASEAN with Merck, GSK, GS1 Global and more! 


  • Updates straight from authorities: ANVISA, Cofepris, and Cuban Regulatory Authority (CECMED)
  • Immerse yourself in case studies on orphan drug registration, APIs and Market Access   
  • Assess how COVID has impacted LATAM regulation with input from CIRS   


  • Get to grips with MENA’s regulatory landscape with industry experts   
  • Join interactive sessions on product registration in the GCC with Astrazenca and Acino   
  • Discuss risk Management with - Head of Iraqi Pharmacovigilance Centre, Ministry of Health Iraq 


  • Keep informed about the latest updates on the Eurasian Economic Union (EAEU)   
  • Learn best practices for product registration from real-life scenarios
  • Understand the latest labelling requirements in EAEU and CIS markets

It's time to overcome your global regulatory hurdles

Connect with pioneers in the pharmaceutical regulatory landscape to help you:

Stay Up-to-Date with Regional Regulation Changes

Feedback Directly from Government Health Authorities and Ministries

Excel in Emerging Regions with Successful Submissions

Effectively Navigate Through Cultural Differences

Successfully Interpret and Investigate the More Challenging Regional Regulations

Understand the Future of Harmonisation