Dublin, May 30, 2025 (GLOBE NEWSWIRE) -- The "Pharmaceutical Regulatory Affairs in Asia Training Course" 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 seminar will be of particular interest to all those who need to learn about successful marketing authorisation applications and in-market regulatory compliance, whether as an introductory or a refresher course.
Previous delegates have included:
- Scientists and technical staff in
- Regulatory affairs
- Registration departments
- Medical directors
The programme consists of regional presentations covering:
- The markets
- Brief commercial and cultural background
- Importance of major markets
- Company and product registration
- Regulations and guidelines
- Drug classification systems
- Site registration
- New products
- Line extensions
- Labelling changes
- Sourcing changes
- Registration samples
- Certificates/legalisation
- Application process
- Committees/meetings
- New applications
- Variations
- Renewals/re-registration
- Recent regulatory developments
- Influences and changes: national and regional
- The latest regulatory developments in the region
For more information about this training visit https://www.researchandmarkets.com/r/v4ynky
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