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
  

Programme

Presenters

Andrew Thornley, UCB Pharma
Claire McDonald, GSK
Alexis Cockroft, Lex Regulatory Ltd

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

Standard

• Member: £580+VAT*
• Non-member: £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

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.