When: 9 April 2025
Where: Lincoln Plaza Hotel, 2 Lincoln Plaza, London E14 9BN
Time: 09:30-16:30 BST
This course is also available to take part in online.
Suitable for
This course is designed for those:
- Who are new to regulatory affairs;
- Who wish to move into the profession;
- Working in related professions (law, pharmaceutical manufacturing, marketing and sales, healthcare, administration, project management);
- Those currently working in regulatory authorities and those in the regulatory sector.
Course information
This popular course provides an opportunity that on-the-job learning doesn't: network and learn from a variety of experts, including your fellow delegates. By attending this course, you will:
- Get a clear understanding of the roles played by regulatory affairs professionals obtaining and maintaining marketing authorisation for medicines
- Learn the key steps involved in developing new pharmaceuticals
- Gain an overview of EU legislative framework and regulatory procedures
- Get insights about the strategies needed to be applied by regulatory affairs professionals to obtain best results for their organisations and stakeholders
- Understand life-cycle management procedures including variations, the essentials of clinical trials and importance of labelling.
Benefits to delegates
- Get a complete grounding in regulatory affairs in just one day
- Be taught by regulatory affairs experts with extensive practical examples
- Understand the regulatory affairs sector and find out for yourself how you can maximise your performance, either as a regulatory professional or working alongside regulatory colleagues
- Build a network to support the rest of your career
CPD: This course provides 6 CPD hours upon successful completion
To learn more about why Continuing Professional Development is important, visit our Lifelong Learning page.
Programme
The draft programme for this course can be downloaded here.
Presenters
Further details will be released in the near future.
Pricing
| Standard training course registration fees |
| Event Registration Type |
Price (GBP) |
Standard Price
TOPRA Member |
£620.00 + VAT* |
Standard Price
Non-member |
£720.00 + 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
|
£465.00 + VAT* |
Government or academic rates
Non-member
|
£540.00 + VAT* |
Charities, patient groups, full-time education rates
TOPRA Member |
£310.00 + VAT* |
Charities, patient groups, full-time education rates
Non-member
|
£360.00 + 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.
Related courses
On-demand webinar: Your Career in Regulatory Affairs - Your First Steps
Essentials of European Pharmaceutical Regulatory Affairs and Essentials of European Medical Devices
Next steps
Introductory courses in regulatory affairs
Terms and conditions
Please read the training terms and conditions before booking this course. By booking a place on this course you are agreeing to the training terms and conditions.