When: 17 March 2022
Location: TOPRA, 3 Harbour Exchange, London, E14 9GE
Time: 09.30-16.30 (GMT)
Also available as a virtual course, please click here for the virtual registration option
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 labeling
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 the programme here
Presenters
- Andy Thornley, UCB Pharma
- Claire McDonald, GSK
- Kasia Nowok, UCB Pharma
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
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%
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