When: 15-17 April 2025
Where: Lincoln Plaza Hotel, 2 Lincoln Plaza, London E14 9BN, UK
Time: Start time Day 1: 08:30 (CET+1) End time Day 3: 16:15 BST (CET+1)
Suitable for
This course is essential for:
- People new to regulatory affairs who want to acquire a comprehensive foundation
- Regulatory professionals wishing to update their knowledge
- Allied professionals wanting to understand the role of regulatory affairs
Note: This course is also Module 0 of the MSc Regulatory Affairs.
Course information
TOPRA's Introductory Courses have been designed to provide a firm foundation to your career in regulatory affairs. They are the most comprehensive of their kind and are presented by speakers and facilitators from industry and agencies, all respected authorities in their field. Our three-day Overview of EU Pharmaceutical Regulatory Affairs course (formerly known as the The Spring Introductory Course) covers all aspects of the product development process and provides a sound overview of EU legislation and regulatory procedures, plus explores the central role regulatory affairs plays in modern healthcare companies and the development cycle of new drugs.
Benefits for delegates
- Three interactive days with comprehensive range of topics and case studies
- Develop a network to support the rest of your career
- Meet and learn from an international speaker panel from agencies, industry and contract houses
- High quality course materials
- Gain the practical skills to be a highly effective regulatory professional
- Industry-wide recognised programme will be an excellent start to your career
CPD: This course provides 15 CPD hours upon successful completion. To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.
Programme
You can view and download the course programme here.
Module Leaders
Presenters
Presenters for this training course include:
- Dima Al-hadithi, CMC & Strategy Consultant
- Mirza Catibušic, Senior Pharmaceutical Assessor, HPRA
- Shaila Choi, Senior Director, AZAFAROS B.V.
- Christine Grew, Director, Canopy Life Sciences
- David Jones, Consultant
- Richard Keane, Senior Director, Biogen
- Kay Martin, Senior Manager Regulatory Affairs, Biogen
- Steve Pinder, Director, Envestia
- Tomáš Radimerský, State Institute of Drug Control, Czechia
Pricing
| Standard training course registration fees |
| Event Registration Type |
Price (GBP) |
Standard Price
TOPRA Member |
£2,200.00 + VAT* |
Standard Price
Non-member |
£2,600.00 + VAT* |
TOPRA MSc Students
|
£1,650.00 + VAT* |
Save on the full cost of membership and £180 on the price of your training
course when you add TOPRA membership to your booking (membership fees are exempt from VAT).
*VAT, where applicable, is charged at the rate of 20%.
| Discounted training course registration fees |
| Event Registration Type |
Price (GBP) |
Government or academic rates
TOPRA Member
|
£1,650.00 + VAT* |
Government or academic rates
Non-member
|
£1,950.00 + VAT* |
Charities, patient groups, full-time education rates
TOPRA Member |
£1,100.00 + VAT* |
Charities, patient groups, full-time education rates
Non-member
|
£1,300.00 + VAT* |
Places are also available for those in low-income countries as defined by the World Bank.
*VAT, where applicable, is charged at the rate of 20%.
Please email meetings@topra.org for a discount code before making your booking.
Terms and conditions
By booking a place on this course you are agreeing to the training terms and conditions.