Date: 6 August 2024
Time: 09:30-16:30
Location: TOPRA 6th Floor, 3 Harbour Exchange, London, E14 9GE
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 labelling
Benefits to delegates
By attending this course you will:
- 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 programme for this course can be downloaded here.
Presenters
Andy Thornley, UK Liason in Global Regulatory Affairs, UCBpharma
Alexis Cockroft, Director and Regulatory Consultant, Lex Regulatory Ltd
Lizzy Heads, Associate Regulatory Affairs Manager, G&LScientific
Yevheniia Prysiazhna, Regulatory Affairs Manager, G&L Healthcare Advisors
David Solomon, Consultant
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 |
£615+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
|
£461.25+VAT
|
Those working for charities, patient groups or in full-time education
|
£307.50+VAT |
|
*VAT, if applicable, is charged at the rate of 20%
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Next steps
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.