Pharmaceutical Regulatory Affairs in Asia Training Course: Important Aspects of Gaining and Maintaining a Successful Marketing Authorisation (Mar 24th – Mar 26th, 2026) – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “Pharmaceutical Regulatory Affairs in Asia Training Course (Mar 24th – Mar 26th, 2026)” training has been added to ResearchAndMarkets.com’s offering.

The pharmaceutical market in Asia is growing at a rapid pace and presents both opportunities and challenges to those wishing to work in the region. Rather than a single market, Asia is a collection of different markets, each with their own regulatory processes, although harmonisation exists within the ASEAN countries.

This seminar will provide a practical overview of the key areas of pharmaceutical regulatory affairs in Asia, including India, and will cover all important aspects of gaining and maintaining a successful marketing authorisation within the region.

The programme will include:

• Discussion of underlying official regulatory sources
• An interpretation of practical aspects
• An overview of the requirements for local manufacturing
• Recent developments
• Harmonisation initiatives
• An update and wider knowledge of regulatory affairs in Asia
• The opportunity to exchange experiences with other delegate

Benefits of attending:

• Gain an overview of key Asian markets
• Discuss outlines of company and product registration
• Understand the application process
• Assess the impact of recent regulatory developments in the region
• Discuss harmonisation initiatives including ASEAN opportunities
• Understand how Japan fits in the Asian regulatory landscape
• Discover general, country-specific and regional requirements

Please note that the course will provide an excellent introduction to all the key aspects of regulatory affairs in the Asia region but will not focus specifically or in detail on Chemistry, Manufacture and Control (CMC).

Certifications:

• CPD: 18 hours for your records
• Certificate of completion

Who Should Attend:

This programme is primarily designed for Pharmaceutical Regulatory Affairs professionals:

• Those interested in working with Asian countries, seeking updates on recent developments, exchanging information, or obtaining guidance on current challenges
• Regulatory Affairs professionals new to the Asian region, requiring extensive background knowledge and training

In addition, the programme may also be of interest to professionals from related functions, such as Marketing, Logistics, Production, and others, who would benefit from a general overview and introduction to Pharmaceutical Regulatory Affairs in Asia.

This programme does not cover Medical Devices, Immunologicals, or Vaccines.

Key Topics Covered:

Day 1

• Introduction to the Asia Region
• Introduction to ASEAN
• Philippines
• Brunei
• PR of China

Day 2

• India
• Malaysia
• Singapore
• Hong Kong
• Indonesia
• Thailand
• Vietnam/Cambodia/Laos

Day 3

• Taiwan
• Korea
• Outline on Japan
• ASEAN Harmonisation

For more information about this training visit https://www.researchandmarkets.com/r/1v01on

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