When: 6 May 2021
Where: Sheraton Brussels Airport Hotel, Brussels National Airport, 1930 Brussels, Belgium (This course is also offered at the same date and time online)
Time: 09:30-15:50 CEST (CET+1) | 08:30-14:50 BST (GMT+1)
Course overview
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
I am very very new to regulatory, and lots of this information helped me to connect the dots in some areas that had previously been confusing.” – 2020 delegate
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
Download a copy of the provisional programme here.
Presenters
To be announced.
Suitable for
This course is designed for those:
- Who are new to regulatory affairs
- Who wish to move into the profession
- From related professions (law, pharmaceutical manufacturing, marketing and sales, healthcare, administration, project management)
- Who would gain by obtaining better insight about the world of their partners in regulatory affairs
- Those who work in regulatory authorities and those in the regulatory sector
Accommodation
A limited number of rooms have been held at a preferential rate at the Sheraton Brussels Airport Hotel where the course is taking place. For more information on how to book, please email sammi.kwok@topra.org.
Pricing
Course fees*:
| Type |
Fee |
| Standard |
£580+VAT |
Discounted places
A limited number of discounted places are available at the rates below.
Please email us at meetings@topra.org for a discount code before making your booking.
|
Those working for regulatory agencies, government agencies or academic institutions
|
£435+VAT
|
Those working for charities, patient groups or in full-time education
|
£290+VAT |
|
*VAT, if applicable, is charged at the rate of 20%
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
Registration
Simply log in or create an account and then register using the 'Register Myself' button that will appear below once you are logged in.