This course is also available to attend online.
When: 24 - 26 February 2026
Where: TOPRA Office, 3rd Floor City Reach, 5-6 Greenwich View Place, London, E14 9NN, UK
Day 1 start time: TBC | Day 3 end time: TBC
CPD: 15 CPD hours upon successful completion
Who should attend
- Students of the TOPRA MSc programme
- Delegates from the pharmaceutical industry who wish to develop their knowledge
- Delegates from allied industries who wish to have a comprehensive understanding of the subject
What you'll learn
By completing this course, you will be able to:
- Demonstrate a critical understanding of the regulatory environment and procedures governing clinical trials and marketing authorisations in South and East Asia
- Analyse and interpret the requirements, documentation, and processes involved in regulatory submissions to regional authorities
- Critically evaluate legal and regulatory documentation, research studies, and scientific communications from diverse sources
- Apply advanced problem-solving and analytical skills to address complex regulatory challenges in drug development
- Assess and synthesise incomplete or conflicting evidence to provide clear, well-reasoned recommendations for both specialist and non-specialist audiences
Course overview
South and East Asia represent some of the most dynamic and diverse regulatory environments in global pharmaceutical development. This course equips regulatory affairs professionals with the knowledge to critically assess the region’s evolving regulatory frameworks, marketing authorisation pathways and clinical trial requirements. Participants will explore legal and procedural variations across countries and consider how these influence global development strategies. Case studies and debates will support the development of effective, context-sensitive regulatory advice for operating in these complex markets.
Course presenters
TOPRA Masterclasses are developed and delivered by a faculty of expert speakers from relevant industry, agencies, notified bodies and other stakeholders, and are validated by the University of Hertfordshire.
Pricing
| Standard training course registration fees |
| Event Registration Type |
Price (GBP) |
Standard Price
TOPRA Member |
£1,750.00 + VAT* |
Standard Price
Non-member |
£2,450.00 + VAT* |
TOPRA MSc Students
|
£1,750.00 + VAT* |
Those working for regulatory or government agencies, academic institutions, charities, patient groups, emerging markets, and MSEs (Micro and Small Enterprises) can also access discounted rates by becoming a TOPRA member. For more information about the discounts available, please email meetings@topra.org before making your booking.
Important Notice On VAT
In compliance with regulations, a *20% VAT will be charged to all attendees, regardless of your country of origin. If you have a VAT number or if the company or organisation you are affiliated with has a VAT number or equivalent please ensure it is visible on your profile. If your VAT number is not visible on your profile, please email finance@topra.org to have it updated. If you do not have a VAT number, there is no action required — VAT will be applied accordingly during the registration process. Please observe that the VAT number needs to be valid.
Click here to check and validate your VAT number.
For EU countries; if you are unsure of the VAT number, click here to check and validate your VAT number.
Terms and conditions
By booking a place on this course you are agreeing to the Training Terms and Conditions.